ClinVar Miner

List of variants in gene SDHA reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 60
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HGVS dbSNP
NM_001294332.1(SDHA):c.-115T>C rs2303741
NM_001294332.1(SDHA):c.-84dup rs35805262
NM_004168.4(SDHA):c.-4A>G rs377134185
NM_004168.4(SDHA):c.-7A>C rs751633537
NM_004168.4(SDHA):c.1026G>A (p.Val342=) rs1060505004
NM_004168.4(SDHA):c.1038C>G (p.Ser346=) rs1041949
NM_004168.4(SDHA):c.1071T>C (p.Cys357=) rs1553999410
NM_004168.4(SDHA):c.113A>T (p.Asp38Val) rs34635677
NM_004168.4(SDHA):c.1140G>A (p.Leu380=) rs146348714
NM_004168.4(SDHA):c.1170C>T (p.Phe390=) rs35277230
NM_004168.4(SDHA):c.1261-4A>T rs1553999703
NM_004168.4(SDHA):c.1305G>C (p.Leu435=) rs35964044
NM_004168.4(SDHA):c.1305G>T (p.Leu435=) rs35964044
NM_004168.4(SDHA):c.1422A>G (p.Ser474=) rs201868424
NM_004168.4(SDHA):c.1432+20G>C rs200127852
NM_004168.4(SDHA):c.1432+7G>C rs760526397
NM_004168.4(SDHA):c.1443C>A (p.Val481=) rs751871185
NM_004168.4(SDHA):c.146A>G (p.Asp49Gly) rs80207011
NM_004168.4(SDHA):c.1476T>C (p.Ser492=) rs1376968004
NM_004168.4(SDHA):c.150+9A>G rs1553997201
NM_004168.4(SDHA):c.1572C>G (p.Ala524=) rs185679709
NM_004168.4(SDHA):c.1599A>G (p.Gln533=) rs1407806818
NM_004168.4(SDHA):c.1614A>G (p.Lys538=) rs1554001847
NM_004168.4(SDHA):c.163T>C (p.Tyr55His) rs142926807
NM_004168.4(SDHA):c.1664-24del rs534296796
NM_004168.4(SDHA):c.1664-4C>G rs774876028
NM_004168.4(SDHA):c.1664-8G>A rs199790689
NM_004168.4(SDHA):c.1680G>A (p.Thr560=) rs1139449
NM_004168.4(SDHA):c.1752A>G (p.Ala584=) rs13070
NM_004168.4(SDHA):c.1776T>C (p.His592=) rs1126538
NM_004168.4(SDHA):c.1794+8T>G rs1050394308
NM_004168.4(SDHA):c.17G>A (p.Gly6Asp) rs187964306
NM_004168.4(SDHA):c.1806T>C (p.Asp602=) rs1554002427
NM_004168.4(SDHA):c.1857G>A (p.Glu619=) rs1247081812
NM_004168.4(SDHA):c.1886A>T (p.Tyr629Phe) rs6960
NM_004168.4(SDHA):c.1908+15C>T rs34504623
NM_004168.4(SDHA):c.1911C>T (p.Val637=) rs11557098
NM_004168.4(SDHA):c.1926A>G (p.Arg642=) rs1554002873
NM_004168.4(SDHA):c.1932G>A (p.Val644=) rs6961
NM_004168.4(SDHA):c.1969G>A (p.Val657Ile) rs6962
NM_004168.4(SDHA):c.1989C>T (p.Ser663=) rs1554002913
NM_004168.4(SDHA):c.309A>G (p.Ala103=) rs1139424
NM_004168.4(SDHA):c.313-19G>T rs185555941
NM_004168.4(SDHA):c.390C>T (p.Ser130=) rs748976493
NM_004168.4(SDHA):c.456+9C>T rs200565489
NM_004168.4(SDHA):c.513T>C (p.Arg171=) rs765157205
NM_004168.4(SDHA):c.549C>T (p.Gly183=) rs61733344
NM_004168.4(SDHA):c.550G>A (p.Gly184Arg) rs148246073
NM_004168.4(SDHA):c.619A>C (p.Arg207=) rs6555055
NM_004168.4(SDHA):c.627G>A (p.Leu209=) rs149821224
NM_004168.4(SDHA):c.64-10G>A rs1553997159
NM_004168.4(SDHA):c.684T>C (p.Asn228=) rs2115272
NM_004168.4(SDHA):c.771-11A>G rs2288461
NM_004168.4(SDHA):c.789C>T (p.Tyr263=) rs1553998616
NM_004168.4(SDHA):c.822C>A (p.Gly274=) rs34771391
NM_004168.4(SDHA):c.822C>T (p.Gly274=) rs34771391
NM_004168.4(SDHA):c.891T>C (p.Pro297=) rs1126417
NM_004168.4(SDHA):c.895+13G>A rs201461936
NM_004168.4(SDHA):c.942G>A (p.Glu314=) rs1553998977
NM_004168.4(SDHA):c.969C>T (p.Gly323=) rs142849100

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