rs56141211

Orientation

plus

Stabilized

plus

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

Make rs56141211(A;A)

Make rs56141211(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

10626447

Gene

GCNT2

is a	snp
is	mentioned by
dbSNP	rs56141211
dbSNP (classic)	rs56141211
ClinGen	rs56141211
ebi	rs56141211
HLI	rs56141211
Exac	rs56141211
Gnomad	rs56141211
Varsome	rs56141211
LitVar	rs56141211
Map	rs56141211
PheGenI	rs56141211
Biobank	rs56141211
1000 genomes	rs56141211
hgdp	rs56141211
ensembl	rs56141211
geneview	rs56141211
scholar	rs56141211
google	rs56141211
pharmgkb	rs56141211
gwascentral	rs56141211
openSNP	rs56141211
23andMe	rs56141211
SNPshot	rs56141211
SNPdbe	rs56141211
MSV3d	rs56141211
GWAS Ctlg	rs56141211

Max Magnitude

0

OMIM	600429
Desc
Variant	0001
Related	also

ClinVar
Risk	rs56141211(A;A)
Alt	rs56141211(A;A)
Reference	Rs56141211(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.10626680G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009699.7,