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rs587777831

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777831(A;G)
Make rs587777831(G;G)
ReferenceGRCh38 38.1/142
Chromosome12
Position14841155
GeneART4
is asnp
is mentioned by
dbSNPrs587777831
ebirs587777831
HLIrs587777831
Exacrs587777831
Varsomers587777831
Maprs587777831
PheGenIrs587777831
hapmaprs587777831
1000 genomesrs587777831
hgdprs587777831
ensemblrs587777831
gopubmedrs587777831
geneviewrs587777831
scholarrs587777831
googlers587777831
pharmgkbrs587777831
gwascentralrs587777831
openSNPrs587777831
23andMers587777831
23andMe allrs587777831
SNP Nexus

SNPshotrs587777831
SNPdbers587777831
MSV3drs587777831
GWAS Ctlgrs587777831
Max Magnitude0
ClinVar
Risk rs587777831(G;G)
Alt rs587777831(G;G)
Reference rs587777831(A;A)
Significance Other
Disease Blood group
Variation info
Gene ART4
CLNDBN Blood group, Dombrock system
Reversed 1
HGVS NC_000012.11:g.14994089T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019305.25,