ClinVar Miner

List of variants in gene SDHAF2 reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_017841.2(SDHAF2):c.*377T>C rs17702
NM_017841.2(SDHAF2):c.*378G>A rs7935377
NM_017841.2(SDHAF2):c.*415A>G rs61132686
NM_017841.2(SDHAF2):c.*456A>G rs6632
NM_017841.2(SDHAF2):c.36+10G>A rs114207859
NM_017841.2(SDHAF2):c.63A>G (p.Leu21=) rs191513932

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