rs1045409136

Orientation

plus

Stabilized

plus

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

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

235489269

Gene

B3GALNT2

is a	snp
is	mentioned by
dbSNP	rs1045409136
dbSNP (classic)	rs1045409136
ClinGen	rs1045409136
ebi	rs1045409136
HLI	rs1045409136
Exac	rs1045409136
Gnomad	rs1045409136
Varsome	rs1045409136
LitVar	rs1045409136
Map	rs1045409136
PheGenI	rs1045409136
Biobank	rs1045409136
1000 genomes	rs1045409136
hgdp	rs1045409136
ensembl	rs1045409136
geneview	rs1045409136
scholar	rs1045409136
google	rs1045409136
pharmgkb	rs1045409136
gwascentral	rs1045409136
openSNP	rs1045409136
23andMe	rs1045409136
SNPshot	rs1045409136
SNPdbe	rs1045409136
MSV3d	rs1045409136
GWAS Ctlg	rs1045409136

Max Magnitude

0

ClinVar
Risk	rs1045409136(T;T)
Alt	rs1045409136(T;T)
Reference	Rs1045409136(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	B3GALNT2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.235652574C>T
CLNSRC
CLNACC	RCV000479796.1,