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rs587777833

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777833(C;C)
Make rs587777833(C;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position14842968
GeneART4
is asnp
is mentioned by
dbSNPrs587777833
ebirs587777833
HLIrs587777833
Exacrs587777833
Varsomers587777833
Maprs587777833
PheGenIrs587777833
hapmaprs587777833
1000 genomesrs587777833
hgdprs587777833
ensemblrs587777833
gopubmedrs587777833
geneviewrs587777833
scholarrs587777833
googlers587777833
pharmgkbrs587777833
gwascentralrs587777833
openSNPrs587777833
23andMers587777833
23andMe allrs587777833
SNP Nexus

SNPshotrs587777833
SNPdbers587777833
MSV3drs587777833
GWAS Ctlgrs587777833
Max Magnitude0
ClinVar
Risk rs587777833(C;C)
Alt rs587777833(C;C)
Reference rs587777833(T;T)
Significance Other
Disease Blood group
Variation info
Gene ART4
CLNDBN Blood group, Dombrock system
Reversed 1
HGVS NC_000012.11:g.14995902A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019307.25,