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rs11461

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs11461(C;T)
Make rs11461(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position124400865
GeneOAT
is asnp
is mentioned by
dbSNPrs11461
ebirs11461
HLIrs11461
Exacrs11461
Varsomers11461
Maprs11461
PheGenIrs11461
hapmaprs11461
1000 genomesrs11461
hgdprs11461
ensemblrs11461
gopubmedrs11461
geneviewrs11461
scholarrs11461
googlers11461
pharmgkbrs11461
gwascentralrs11461
openSNPrs11461
23andMers11461
23andMe allrs11461
SNP Nexus

SNPshotrs11461
SNPdbers11461
MSV3drs11461
GWAS Ctlgrs11461
GMAF0.4109
Max Magnitude0
OMIM258870
DescOAT POLYMORPHISM
Variant0017
Relatedalso
OMIM613349
Desc
Variant0017
Relatedalso
ClinVar
Risk rs11461(T;T)
Alt rs11461(T;T)
Reference rs11461(C;C)
Significance Non-pathogenic
Disease OAT POLYMORPHISM
Variation info
Gene OAT
CLNDBN OAT POLYMORPHISM
Reversed 1
HGVS NC_000010.10:g.126089434G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000184.1,