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rs56340844

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs56340844(C;T)
Make rs56340844(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position14840856
GeneART4
is asnp
is mentioned by
dbSNPrs56340844
ebirs56340844
HLIrs56340844
Exacrs56340844
Varsomers56340844
Maprs56340844
PheGenIrs56340844
hapmaprs56340844
1000 genomesrs56340844
hgdprs56340844
ensemblrs56340844
gopubmedrs56340844
geneviewrs56340844
scholarrs56340844
googlers56340844
pharmgkbrs56340844
gwascentralrs56340844
openSNPrs56340844
23andMers56340844
23andMe allrs56340844
SNP Nexus

SNPshotrs56340844
SNPdbers56340844
MSV3drs56340844
GWAS Ctlgrs56340844
Max Magnitude0
OMIM110600
Desc
Variant0005
Relatedalso
ClinVar
Risk rs56340844(T;T)
Alt rs56340844(T;T)
Reference rs56340844(C;C)
Significance Other
Disease Blood group
Variation info
Gene ART4
CLNDBN Blood group, Dombrock system
Reversed 1
HGVS NC_000012.11:g.14993790G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000019308.29,