List of variants in gene B4GAT1 reported as likely benign 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_006876.3(B4GAT1):c.987C>T (p.Tyr329=)	rs1190625	0.00264
NM_006876.3(B4GAT1):c.69G>C (p.Ala23=)	rs146812867	0.00059
NM_006876.3(B4GAT1):c.510C>G (p.Pro170=)	rs761777602	0.00005
NM_006876.3(B4GAT1):c.300C>T (p.His100=)	rs746274346	0.00002
NM_006876.3(B4GAT1):c.1152C>G (p.Pro384=)
NM_006876.3(B4GAT1):c.534G>T (p.Leu178=)
NM_006876.3(B4GAT1):c.720G>C (p.Leu240=)
NM_006876.3(B4GAT1):c.756C>A (p.Gly252=)

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