ClinVar Miner

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

Included ClinVar conditions (123):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_017841.4(SDHAF2):c.*113C>A rs886048416
NM_017841.4(SDHAF2):c.*170C>A rs886048417
NM_017841.4(SDHAF2):c.*172del rs537244040
NM_017841.4(SDHAF2):c.*627G>T rs886048422
NM_017841.4(SDHAF2):c.*653A>G rs886048423
NM_017841.4(SDHAF2):c.370+12G>A rs886048415

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