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rs121909545

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909545(C;G)
Make rs121909545(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position35176643
GeneCD44
is asnp
is mentioned by
dbSNPrs121909545
ebirs121909545
HLIrs121909545
Exacrs121909545
Varsomers121909545
Maprs121909545
PheGenIrs121909545
hapmaprs121909545
1000 genomesrs121909545
hgdprs121909545
ensemblrs121909545
gopubmedrs121909545
geneviewrs121909545
scholarrs121909545
googlers121909545
pharmgkbrs121909545
gwascentralrs121909545
openSNPrs121909545
23andMers121909545
23andMe allrs121909545
SNP Nexus

SNPshotrs121909545
SNPdbers121909545
MSV3drs121909545
GWAS Ctlgrs121909545
Max Magnitude0
OMIM107269
Desc
Variant0001
Relatedalso
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,