List of variants in gene GALT reported as likely benign for not specified

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000155.4(GALT):c.329-24G>A	rs114539202	0.00175
NM_000155.4(GALT):c.687+9G>C	rs117998880	0.00057
NM_000155.4(GALT):c.498T>C (p.Pro166=)	rs193922249	0.00029
NM_000155.4(GALT):c.564+15G>A	rs111033732	0.00015
NM_000155.4(GALT):c.1128A>T (p.Ala376=)	rs781374930	0.00006
NM_000155.4(GALT):c.799C>T (p.Leu267=)	rs764006034	0.00002
NM_000155.4(GALT):c.1017C>T (p.Tyr339=)	rs759417724	0.00001
NM_000155.4(GALT):c.390C>T (p.Cys130=)	rs1410761611	0.00001
NM_000155.4(GALT):c.564+7G>A	rs760189807	0.00001
NM_000155.4(GALT):c.678A>G (p.Leu226=)	rs777577533	0.00001
NM_000155.4(GALT):c.753C>T (p.Tyr251=)	rs367543261	0.00001
NM_000155.4(GALT):c.762G>A (p.Leu254=)	rs748639317	0.00001
NM_000155.4(GALT):c.83-46G>C	rs201156392
NM_000155.4(GALT):c.885C>G (p.Pro295=)	rs1554709446

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