ClinVar Miner

List of variants in gene SDHAF2 studied for cardiovascular organ benign neoplasm

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP
NM_017841.2(SDHAF2):c.*113C>A rs886048416
NM_017841.2(SDHAF2):c.*12C>T rs113652589
NM_017841.2(SDHAF2):c.*170C>A rs886048417
NM_017841.2(SDHAF2):c.*172del rs537244040
NM_017841.2(SDHAF2):c.*233C>T rs886048419
NM_017841.2(SDHAF2):c.*377T>C rs17702
NM_017841.2(SDHAF2):c.*378G>A rs7935377
NM_017841.2(SDHAF2):c.*389C>T rs886048420
NM_017841.2(SDHAF2):c.*415A>G rs61132686
NM_017841.2(SDHAF2):c.*446C>G rs886048421
NM_017841.2(SDHAF2):c.*456A>G rs6632
NM_017841.2(SDHAF2):c.*49A>G rs549312009
NM_017841.2(SDHAF2):c.*58G>A rs754124809
NM_017841.2(SDHAF2):c.*627G>T rs886048422
NM_017841.2(SDHAF2):c.*653A>G rs886048423
NM_017841.2(SDHAF2):c.*669A>G rs747631379
NM_017841.2(SDHAF2):c.*76C>T rs112750991
NM_017841.2(SDHAF2):c.330C>A (p.Asn110Lys) rs779335034
NM_017841.2(SDHAF2):c.36+10G>A rs114207859
NM_017841.2(SDHAF2):c.370+12G>A rs886048415
NM_017841.2(SDHAF2):c.63A>G (p.Leu21=) rs191513932
NM_017841.2(SDHAF2):c.97C>T (p.Arg33Cys) rs144867876

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