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rs121909386

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909386(C;T)
Make rs121909386(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position89438899
GeneSLC16A12
is asnp
is mentioned by
dbSNPrs121909386
ebirs121909386
HLIrs121909386
Exacrs121909386
Varsomers121909386
Maprs121909386
PheGenIrs121909386
hapmaprs121909386
1000 genomesrs121909386
hgdprs121909386
ensemblrs121909386
gopubmedrs121909386
geneviewrs121909386
scholarrs121909386
googlers121909386
pharmgkbrs121909386
gwascentralrs121909386
openSNPrs121909386
23andMers121909386
23andMe allrs121909386
SNP Nexus

SNPshotrs121909386
SNPdbers121909386
MSV3drs121909386
GWAS Ctlgrs121909386
Max Magnitude0
OMIM611910
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909386(T;T)
Alt rs121909386(T;T)
Reference rs121909386(C;C)
Significance Pathogenic
Disease Cataract
Variation info
Gene SLC16A12
CLNDBN Cataract, juvenile, with microcornea and glucosuria
Reversed 1
HGVS NC_000010.10:g.91198656G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000820.5,