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rs121912761

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912761(C;T)
Make rs121912761(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position126656303
GeneGYPC
is asnp
is mentioned by
dbSNPrs121912761
ebirs121912761
HLIrs121912761
Exacrs121912761
Varsomers121912761
Maprs121912761
PheGenIrs121912761
hapmaprs121912761
1000 genomesrs121912761
hgdprs121912761
ensemblrs121912761
gopubmedrs121912761
geneviewrs121912761
scholarrs121912761
googlers121912761
pharmgkbrs121912761
gwascentralrs121912761
openSNPrs121912761
23andMers121912761
23andMe allrs121912761
SNP Nexus

SNPshotrs121912761
SNPdbers121912761
MSV3drs121912761
GWAS Ctlgrs121912761
Max Magnitude0
OMIM110750
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121912761(T;T)
Alt rs121912761(T;T)
Reference rs121912761(C;C)
Significance Other
Disease Blood group
Variation info
Gene GYPC
CLNDBN Blood group, Gerbich system
Reversed 0
HGVS NC_000002.11:g.127413879C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019302.29,