rs121909545

plus

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

Make rs121909545(C;G)

Make rs121909545(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

35176643

Gene

CD44

is a	snp
is	mentioned by
dbSNP	rs121909545
dbSNP (classic)	rs121909545
ClinGen	rs121909545
ebi	rs121909545
HLI	rs121909545
Exac	rs121909545
Gnomad	rs121909545
Varsome	rs121909545
LitVar	rs121909545
Map	rs121909545
PheGenI	rs121909545
Biobank	rs121909545
1000 genomes	rs121909545
hgdp	rs121909545
ensembl	rs121909545
geneview	rs121909545
scholar	rs121909545
google	rs121909545
pharmgkb	rs121909545
gwascentral	rs121909545
openSNP	rs121909545
23andMe	rs121909545
SNPshot	rs121909545
SNPdbe	rs121909545
MSV3d	rs121909545
GWAS Ctlg	rs121909545

Max Magnitude

0

This is currently incorrectly listed in OMIM (and therefore in ClinVar and other databases) as the CD44 gene polymorphism that causes the In(b-) phenotype (of the Indian blood group system). The correct variant is actually rs369473842.

OMIM	107269
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121909545(G;G)
Alt	rs121909545(G;G)
Reference	Rs121909545(C;C)
Significance	Non-pathogenic
Disease	INDIAN BLOOD GROUP SYSTEM POLYMORPHISM
Variation	info
Gene	CD44
CLNDBN	INDIAN BLOOD GROUP SYSTEM POLYMORPHISM
Reversed	0
HGVS	NC_000011.9:g.35198190C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000019669.3,