ClinVar Miner

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

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP
NM_004168.4(SDHA):c.1064+1G>T
NM_004168.4(SDHA):c.1064+2T>A rs1553999072
NM_004168.4(SDHA):c.1261-2A>G
NM_004168.4(SDHA):c.1432+1G>C rs878854628
NM_004168.4(SDHA):c.1432_1432+1del rs878854627
NM_004168.4(SDHA):c.150+1G>A rs1057523165
NM_004168.4(SDHA):c.1534C>T (p.Arg512Ter) rs748089700
NM_004168.4(SDHA):c.1663+1G>T rs766667009
NM_004168.4(SDHA):c.1765C>T (p.Arg589Trp) rs387906780
NM_004168.4(SDHA):c.1A>G (p.Met1Val) rs1061517
NM_004168.4(SDHA):c.1A>T (p.Met1Leu) rs1061517
NM_004168.4(SDHA):c.210dup (p.Gly71fs) rs1553997340
NM_004168.4(SDHA):c.2T>A (p.Met1Lys)
NM_004168.4(SDHA):c.2T>C (p.Met1Thr) rs750380279
NM_004168.4(SDHA):c.2T>G (p.Met1Arg) rs750380279
NM_004168.4(SDHA):c.457-2_457del rs878854632
NM_004168.4(SDHA):c.622-1G>A rs1285132774
NM_004168.4(SDHA):c.63+2del
NM_004168.4(SDHA):c.757_758del (p.Val253fs) rs1553998254

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