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  • Muscular Dystrophy: Genomapp

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    Brea Gunter
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    This document reports the results of a genetic test for markers associated with muscular dystrophy. It finds that the individual has one copy of a variant reported as likely pathogenic for muscular dystrophy. However, they do not have any copies of 14 other variants reported as pathogenic or likely pathogenic for various forms of muscular dystrophy. It concludes by reminding that the information provided is not for diagnostic use.

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    genomappAnces_Musculardystrophy_202011031736

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    This document reports the results of a genetic test for markers associated with muscular dystrophy. It finds that the individual has one copy of a variant reported as likely pathogenic for muscular dystrophy. However, they do not have any copies of 14 other variants reported as pathogenic or likely pathogenic for various forms of muscular dystrophy. It concludes by reminding that the information provided is not for diagnostic use.

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    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
    Flag for inappropriate content
    11 views3 pages

    Muscular Dystrophy: Genomapp

    Uploaded by

    Brea Gunter
    This document reports the results of a genetic test for markers associated with muscular dystrophy. It finds that the individual has one copy of a variant reported as likely pathogenic for muscular dystrophy. However, they do not have any copies of 14 other variants reported as pathogenic or likely pathogenic for various forms of muscular dystrophy. It concludes by reminding that the information provided is not for diagnostic use.

    Copyright:

    © All Rights Reserved
    Download as PDF, TXT or read online from Scribd
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    of 3

    Genomapp v 5.8.

    22 Android November 3, 2020 File #2 (Ancestry) 1

    Complex Diseases - With likely pathogenic markers

    Muscular dystrophy

    You may have a slightly higher gene c suscep bility to develop the
    condi on.

    Markers found in your provided file


    A G ! rs28936415 G G rs59332535

    You have one copy of the variant You have no copy of the allele
    associated with the condi on. This associated with the condi on. The
    variant has been reported as Likely results of the variant don't affect you.
    pathogenic. This variant has been reported as
    Pathogenic.
    PMM2
    LMNA

    G G rs267607634 C C rs58932704

    You have no copy of the allele You have no copy of the allele
    associated with the condi on. The associated with the condi on. The
    results of the variant don't affect you. results of the variant don't affect you.
    This variant has been reported as This variant has been reported as
    Pathogenic. Pathogenic.

    LMNA LMNA

    Please, remember that informa on on this page is not for diagnos c use.
    Genomapp v 5.8.22 Android November 3, 2020 File #2 (Ancestry) 2

    C C rs142336618 T T rs200198778

    You have no copy of the allele You have no copy of the allele
    associated with the condi on. The associated with the condi on. The
    results of the variant don't affect you. results of the variant don't affect you.
    This variant has been reported as This variant has been reported as
    Pathogenic. Pathogenic.

    GMPPB POMT2

    C C rs387907298 A A rs121908110

    You have no copy of the allele You have no copy of the allele
    associated with the condi on. The associated with the condi on. The
    results of the variant don't affect you. results of the variant don't affect you.
    This variant has been reported as This variant has been reported as
    Pathogenic. Pathogenic.

    SGCA FKRP

    T T rs267607644 G G rs34997054

    You have no copy of the allele You have no copy of the allele
    associated with the condi on. The associated with the condi on. The
    results of the variant don't affect you. results of the variant don't affect you.
    This variant has been reported as This variant has been reported as
    Likely pathogenic. Likely pathogenic.

    LMNA DYSF

    Please, remember that informa on on this page is not for diagnos c use.
    Genomapp v 5.8.22 Android November 3, 2020 File #2 (Ancestry) 3

    C C rs397517497 C C rs151244052

    You have no copy of the allele You have no copy of the allele
    associated with the condi on. The associated with the condi on. The
    results of the variant don't affect you. results of the variant don't affect you.
    This variant has been reported as This variant has been reported as
    Likely pathogenic. Likely benign.

    TTN DMD

    Please, remember that informa on on this page is not for diagnos c use.

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