ClinVar Miner

List of variants reported as likely benign for hereditary gallbladder disorder

Included ClinVar conditions (6):

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)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_022437.3(ABCG8):c.491G>A (p.Arg164Gln)	rs74358901	0.00232
NM_022437.3(ABCG8):c.384G>A (p.Lys128=)	rs764690028	0.00016

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