List of variants in gene B3GALNT2 reported by CeGaT Center for Human Genetics Tuebingen

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_152490.5(B3GALNT2):c.1215C>T (p.Pro405=)	rs145518904	0.00029
NM_152490.5(B3GALNT2):c.465C>T (p.Ile155=)	rs138058326	0.00022
NM_152490.5(B3GALNT2):c.169G>A (p.Val57Met)	rs142756842	0.00016
NM_152490.5(B3GALNT2):c.397G>A (p.Glu133Lys)	rs146090744	0.00004
NM_152490.5(B3GALNT2):c.1089C>T (p.Leu363=)	rs1057522976	0.00001
NM_152490.5(B3GALNT2):c.1A>G (p.Met1Val)	rs763641118	0.00001
NM_152490.5(B3GALNT2):c.411G>A (p.Ser137=)	rs1443841724	0.00001
NM_152490.5(B3GALNT2):c.1234T>G (p.Cys412Gly)	rs1486202893
NM_152490.5(B3GALNT2):c.874C>T (p.Arg292Cys)	rs1683282264

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