ClinVar Miner

List of variants in gene SDHAF2 reported as uncertain significance for cardiovascular organ benign neoplasm

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP
NM_017841.2(SDHAF2):c.*113C>A rs886048416
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.*389C>T rs886048420
NM_017841.2(SDHAF2):c.*446C>G rs886048421
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.330C>A (p.Asn110Lys) rs779335034
NM_017841.2(SDHAF2):c.370+12G>A rs886048415

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