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rs1008708453

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 2 O2 alleles (ABO Type O) may be present
(A;C) 2 O2 ABO (type O) allele may be present
Make rs1008708453(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position133262144
GeneABO
is asnp
is mentioned by
dbSNPrs1008708453
dbSNP (old)rs1008708453
ClinGenrs1008708453
ebirs1008708453
HLIrs1008708453
Exacrs1008708453
Gnomadrs1008708453
Varsomers1008708453
Maprs1008708453
PheGenIrs1008708453
Biobankrs1008708453
1000 genomesrs1008708453
hgdprs1008708453
ensemblrs1008708453
gopubmedrs1008708453
geneviewrs1008708453
scholarrs1008708453
googlers1008708453
pharmgkbrs1008708453
gwascentralrs1008708453
openSNPrs1008708453
23andMers1008708453
23andMe allrs1008708453
SNPshotrs1008708453
SNPdbers1008708453
MSV3drs1008708453
GWAS Ctlgrs1008708453
Max Magnitude2
ABO gene variant, known more commonly as c.53G>T or p.Arg18Leu.

The rs1008708453(A) allele, as represented in dbSNP (and SNPedia) on the forward/plus strand, is reported to be completely correlated to a subtype of O type alleles known as the O2 group. These O alleles may lack the c.261delG allele that is associated with the majority of O alleles.[PMID 11155073]

Note that at this position, there is another variant, c.53G>A (p.Arg18Gln), which is not reported to have any particular ABO allelic association as far as we know.