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rs121434508

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121434508(C;T)
Make rs121434508(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position85654139
GeneTMEM126A
is asnp
is mentioned by
dbSNPrs121434508
ebirs121434508
HLIrs121434508
Exacrs121434508
Varsomers121434508
Maprs121434508
PheGenIrs121434508
hapmaprs121434508
1000 genomesrs121434508
hgdprs121434508
ensemblrs121434508
gopubmedrs121434508
geneviewrs121434508
scholarrs121434508
googlers121434508
pharmgkbrs121434508
gwascentralrs121434508
openSNPrs121434508
23andMers121434508
23andMe allrs121434508
SNP Nexus

SNPshotrs121434508
SNPdbers121434508
MSV3drs121434508
GWAS Ctlgrs121434508
GMAF0.0004591
Max Magnitude0
OMIM612988
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434508(T;T)
Alt rs121434508(T;T)
Reference Rs121434508(C;C)
Significance Pathogenic
Disease Optic atrophy 7
Variation info
Gene TMEM126A
CLNDBN Optic atrophy 7
Reversed 0
HGVS NC_000011.9:g.85365183C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000438.3,