List of variants in gene B4GALT7 reported as likely benign by GeneDx

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: 24

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HGVS	dbSNP	gnomAD frequency
NM_007255.2(B4GALT7):c.-413C>A	rs111484007	0.00908
NM_007255.3(B4GALT7):c.640-266G>A	rs73804374	0.00642
NM_007255.3(B4GALT7):c.413+212G>A	rs73337774	0.00436
NM_007255.3(B4GALT7):c.411C>T (p.Phe137=)	rs142951817	0.00140
NM_007255.3(B4GALT7):c.723+20G>A	rs199543624	0.00073
NM_007255.3(B4GALT7):c.387C>T (p.Tyr129=)	rs200124872	0.00047
NM_007255.3(B4GALT7):c.564G>A (p.Pro188=)	rs115756833	0.00028
NM_007255.3(B4GALT7):c.723+19C>T	rs374080326	0.00028
NM_007255.3(B4GALT7):c.867T>C (p.Thr289=)	rs201616836	0.00021
NM_007255.3(B4GALT7):c.498G>A (p.Leu166=)	rs140848441	0.00016
NM_007255.3(B4GALT7):c.589A>G (p.Lys197Glu)	rs200732558	0.00016
NM_007255.3(B4GALT7):c.687C>T (p.Asp229=)	rs756942664	0.00015
NM_007255.3(B4GALT7):c.717G>C (p.Gly239=)	rs149805079	0.00012
NM_007255.3(B4GALT7):c.315C>T (p.Phe105=)	rs150487733	0.00006
NM_007255.3(B4GALT7):c.432C>T (p.Leu144=)	rs369974140	0.00006
NM_007255.3(B4GALT7):c.522C>T (p.Asp174=)	rs775207945	0.00006
NM_007255.3(B4GALT7):c.225C>T (p.Cys75=)	rs780427259	0.00004
NM_007255.3(B4GALT7):c.69C>T (p.Gly23=)	rs759998518	0.00002
NM_007255.3(B4GALT7):c.813C>T (p.Ile271=)	rs570926723	0.00001
NM_007255.3(B4GALT7):c.333C>T (p.Phe111=)	rs750271941
NM_007255.3(B4GALT7):c.414-181T>G	rs116372418
NM_007255.3(B4GALT7):c.51-11G>A	rs763444666
NM_007255.3(B4GALT7):c.51-20C>T	rs1554126437
NM_007255.3(B4GALT7):c.555G>C (p.Val185=)	rs1554126778

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