ClinVar Miner

List of variants reported as benign for hemophagocytic syndrome by Mendelics

Included ClinVar conditions (12):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001083116.3(PRF1):c.11G>A (p.Arg4His)	rs35418374	0.02616
NM_006949.4(STXBP2):c.1298C>T (p.Ala433Val)	rs141309384	0.00866
NM_000081.4(LYST):c.7229+50CTTTT[7]	rs71174459

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