rs137853339

Orientation

plus

Stabilized

plus

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

Make rs137853339(A;A)

Make rs137853339(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

10529416

Gene

GCNT2

is a	snp
is	mentioned by
dbSNP	rs137853339
dbSNP (classic)	rs137853339
ClinGen	rs137853339
ebi	rs137853339
HLI	rs137853339
Exac	rs137853339
Gnomad	rs137853339
Varsome	rs137853339
LitVar	rs137853339
Map	rs137853339
PheGenI	rs137853339
Biobank	rs137853339
1000 genomes	rs137853339
hgdp	rs137853339
ensembl	rs137853339
geneview	rs137853339
scholar	rs137853339
google	rs137853339
pharmgkb	rs137853339
gwascentral	rs137853339
openSNP	rs137853339
23andMe	rs137853339
SNPshot	rs137853339
SNPdbe	rs137853339
MSV3d	rs137853339
GWAS Ctlg	rs137853339

Max Magnitude

0

OMIM	600429
Desc
Variant	0004
Related	also

ClinVar
Risk	rs137853339(A;A)
Alt	rs137853339(A;A)
Reference	Rs137853339(G;G)
Significance	Pathogenic
Disease	I blood group system
Variation	info
Gene	GCNT2
CLNDBN	I blood group system
Reversed	0
HGVS	NC_000006.11:g.10529649G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000009702.8,