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rs55722397

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs55722397(C;G)
Make rs55722397(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position133256031
GeneABO
is asnp
is mentioned by
dbSNPrs55722397
ebirs55722397
HLIrs55722397
Exacrs55722397
Varsomers55722397
Maprs55722397
PheGenIrs55722397
hapmaprs55722397
1000 genomesrs55722397
hgdprs55722397
ensemblrs55722397
gopubmedrs55722397
geneviewrs55722397
scholarrs55722397
googlers55722397
pharmgkbrs55722397
gwascentralrs55722397
openSNPrs55722397
23andMers55722397
23andMe allrs55722397
SNP Nexus

SNPshotrs55722397
SNPdbers55722397
MSV3drs55722397
GWAS Ctlgrs55722397
Max Magnitude0
OMIM110300
Desc
Variant0005
Relatedalso
ClinVar
Risk rs55722397(G;G)
Alt rs55722397(G;G)
Reference rs55722397(C;C)
Significance Other
Disease ABO blood group system
Variation info
Gene ABO
CLNDBN ABO blood group system
Reversed 1
HGVS NC_000009.11:g.136131418G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019313.29,