ClinVar Miner

List of variants in gene combination GFM2, HEXB reported by Counsyl

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_032380.5(GFM2):c.2296C>T (p.Gln766Ter)	rs1407085233	0.00001
NM_032380.5(GFM2):c.2230C>T (p.Arg744Ter)	rs35080306
NM_032380.5(GFM2):c.2239dup (p.Thr747fs)	rs1554037537

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