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rs121912760

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121912760(A;G)
Make rs121912760(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position126656286
GeneGYPC
is asnp
is mentioned by
dbSNPrs121912760
ebirs121912760
HLIrs121912760
Exacrs121912760
Varsomers121912760
Maprs121912760
PheGenIrs121912760
hapmaprs121912760
1000 genomesrs121912760
hgdprs121912760
ensemblrs121912760
gopubmedrs121912760
geneviewrs121912760
scholarrs121912760
googlers121912760
pharmgkbrs121912760
gwascentralrs121912760
openSNPrs121912760
23andMers121912760
23andMe allrs121912760
SNP Nexus

SNPshotrs121912760
SNPdbers121912760
MSV3drs121912760
GWAS Ctlgrs121912760
Max Magnitude0
OMIM110750
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121912760(G;G)
Alt rs121912760(G;G)
Reference rs121912760(A;A)
Significance Other
Disease Blood group
Variation info
Gene GYPC
CLNDBN Blood group, Gerbich system
Reversed 0
HGVS NC_000002.11:g.127413862A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019300.25,