rs201822310

Orientation

plus

Stabilized

plus

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

Make rs201822310(C;G)

Make rs201822310(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

235470869

Gene

B3GALNT2

is a	snp
is	mentioned by
dbSNP	rs201822310
dbSNP (classic)	rs201822310
ClinGen	rs201822310
ebi	rs201822310
HLI	rs201822310
Exac	rs201822310
Gnomad	rs201822310
Varsome	rs201822310
LitVar	rs201822310
Map	rs201822310
PheGenI	rs201822310
Biobank	rs201822310
1000 genomes	rs201822310
hgdp	rs201822310
ensembl	rs201822310
geneview	rs201822310
scholar	rs201822310
google	rs201822310
pharmgkb	rs201822310
gwascentral	rs201822310
openSNP	rs201822310
23andMe	rs201822310
SNPshot	rs201822310
SNPdbe	rs201822310
MSV3d	rs201822310
GWAS Ctlg	rs201822310

Max Magnitude

0

ClinVar
Risk	rs201822310(G;G)
Alt	rs201822310(G;G)
Reference	Rs201822310(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	B3GALNT2
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.235634183C>G
CLNSRC
CLNACC	RCV000490097.1,