List of variants in gene GALNT12 reported as benign by Ambry Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_024642.5(GALNT12):c.356A>T (p.Glu119Val)	rs1137654	0.06543
NM_024642.5(GALNT12):c.897A>G (p.Gln299=)	rs16917929	0.04000
NM_024642.5(GALNT12):c.136G>A (p.Gly46Arg)	rs10987768	0.02982
NM_024642.5(GALNT12):c.1605+4G>A	rs79574929	0.01136
NM_024642.5(GALNT12):c.781G>A (p.Asp261Asn)	rs41306504	0.01010
NM_024642.5(GALNT12):c.359G>C (p.Arg120Pro)	rs202137559	0.00045
NM_024642.5(GALNT12):c.1707G>C (p.Ser569=)	rs2273846

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