ClinVar Miner

List of variants in gene GDAP1 reported as uncertain significance for Charcot-Marie-Tooth disease type 2

Included ClinVar conditions (61):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 63
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HGVS dbSNP
NM_001362931.2(GDAP1):c.694+3856A>G
NM_001362931.2(GDAP1):c.694+3989C>T
NM_001362931.2(GDAP1):c.694+4016T>C
NM_001362931.2(GDAP1):c.694+4037T>C rs886063119
NM_018972.4(GDAP1):c.*1030T>C rs576789317
NM_018972.4(GDAP1):c.*1043G>C
NM_018972.4(GDAP1):c.*1080G>A
NM_018972.4(GDAP1):c.*1124G>T rs886063111
NM_018972.4(GDAP1):c.*1141C>T
NM_018972.4(GDAP1):c.*1165C>G
NM_018972.4(GDAP1):c.*1183G>A
NM_018972.4(GDAP1):c.*1289T>C
NM_018972.4(GDAP1):c.*1301A>G
NM_018972.4(GDAP1):c.*1372A>G
NM_018972.4(GDAP1):c.*1377C>T rs886063112
NM_018972.4(GDAP1):c.*1415C>T
NM_018972.4(GDAP1):c.*1416G>A rs575631045
NM_018972.4(GDAP1):c.*1430T>A rs538689570
NM_018972.4(GDAP1):c.*1437A>C rs557040712
NM_018972.4(GDAP1):c.*1527G>A rs886063113
NM_018972.4(GDAP1):c.*1570G>C rs886063114
NM_018972.4(GDAP1):c.*1779G>T rs886063115
NM_018972.4(GDAP1):c.*18C>T
NM_018972.4(GDAP1):c.*1905A>G
NM_018972.4(GDAP1):c.*1923C>T rs886063116
NM_018972.4(GDAP1):c.*195T>C
NM_018972.4(GDAP1):c.*1968C>T
NM_018972.4(GDAP1):c.*1976C>T rs527937918
NM_018972.4(GDAP1):c.*2125A>C
NM_018972.4(GDAP1):c.*2170A>G rs886063117
NM_018972.4(GDAP1):c.*2210C>T rs571939530
NM_018972.4(GDAP1):c.*2298A>C
NM_018972.4(GDAP1):c.*2298A>G rs4551344
NM_018972.4(GDAP1):c.*331C>T
NM_018972.4(GDAP1):c.*444A>G rs113377784
NM_018972.4(GDAP1):c.*451C>T
NM_018972.4(GDAP1):c.*618C>T rs886063106
NM_018972.4(GDAP1):c.*644G>T
NM_018972.4(GDAP1):c.*663T>C rs886063107
NM_018972.4(GDAP1):c.*697A>G
NM_018972.4(GDAP1):c.*751A>G rs544136357
NM_018972.4(GDAP1):c.*858G>T rs761964880
NM_018972.4(GDAP1):c.*860T>C
NM_018972.4(GDAP1):c.*864G>C rs886063108
NM_018972.4(GDAP1):c.*873T>C rs573385308
NM_018972.4(GDAP1):c.*898A>G rs886063109
NM_018972.4(GDAP1):c.*926C>A
NM_018972.4(GDAP1):c.*931A>G rs532787830
NM_018972.4(GDAP1):c.*961G>C rs886063110
NM_018972.4(GDAP1):c.1006G>T (p.Ala336Ser) rs140811185
NM_018972.4(GDAP1):c.1039A>G (p.Met347Val)
NM_018972.4(GDAP1):c.296A>T (p.Gln99Leu)
NM_018972.4(GDAP1):c.374G>A (p.Arg125Gln) rs771810975
NM_018972.4(GDAP1):c.471T>G (p.Thr157=)
NM_018972.4(GDAP1):c.485-6T>C rs763802909
NM_018972.4(GDAP1):c.556A>G (p.Ile186Val) rs148508128
NM_018972.4(GDAP1):c.602A>G (p.Asn201Ser) rs1586806110
NM_018972.4(GDAP1):c.693A>T (p.Pro231=) rs181157785
NM_018972.4(GDAP1):c.719G>C (p.Cys240Ser)
NM_018972.4(GDAP1):c.776A>G (p.Lys259Arg) rs778557691
NM_018972.4(GDAP1):c.802_803del (p.Trp268fs) rs765346218
NM_018972.4(GDAP1):c.872A>G (p.Lys291Arg)
NM_018972.4(GDAP1):c.965C>T (p.Thr322Met) rs199529910

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