rs367543075

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;-)	0	common in clinvar

Make rs367543075(-;TT)

Make rs367543075(TT;TT)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

235465651

Gene

B3GALNT2

is a	snp
is	mentioned by
dbSNP	rs367543075
dbSNP (classic)	rs367543075
ClinGen	rs367543075
ebi	rs367543075
HLI	rs367543075
Exac	rs367543075
Gnomad	rs367543075
Varsome	rs367543075
LitVar	rs367543075
Map	rs367543075
PheGenI	rs367543075
Biobank	rs367543075
1000 genomes	rs367543075
hgdp	rs367543075
ensembl	rs367543075
geneview	rs367543075
scholar	rs367543075
google	rs367543075
pharmgkb	rs367543075
gwascentral	rs367543075
openSNP	rs367543075
23andMe	rs367543075
SNPshot	rs367543075
SNPdbe	rs367543075
MSV3d	rs367543075
GWAS Ctlg	rs367543075

Max Magnitude

0

ClinVar
Risk	rs367543075(TT;TT)
Alt	rs367543075(TT;TT)
Reference	Rs367543075(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	B3GALNT2
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.235628969_235628970dupAA
CLNSRC
CLNACC	RCV000119390.1,