ClinVar Miner

List of variants reported as likely pathogenic for chromosome 10 disorder by 3billion, Medical Genetics

Included ClinVar conditions (8):

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001002295.2(GATA3):c.1099C>T (p.Arg367Ter)	rs104894164
NM_016628.5(WAC):c.438del (p.Tyr147fs)	rs2132669171
NM_016628.5(WAC):c.610+2T>G

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