List of variants in gene GALT reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000155.4(GALT):c.940A>G (p.Asn314Asp)	rs2070074	0.07150
NM_000155.3(GALT):c.-88G>A	rs144505931	0.00042
NM_000155.4(GALT):c.270T>C (p.Asp90=)	rs1300102277	0.00004
NM_000155.4(GALT):c.1017C>T (p.Tyr339=)	rs759417724	0.00001
NM_000155.4(GALT):c.753C>T (p.Tyr251=)	rs367543261	0.00001
NM_000155.4(GALT):c.*5G>A
NM_000155.4(GALT):c.414G>T (p.Thr138=)	rs116479817
NM_000155.4(GALT):c.508-37C>T
NM_000155.4(GALT):c.83-46G>C	rs201156392

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