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rs141772938

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs141772938(C;G)
Make rs141772938(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position41507837
GeneACO2
is asnp
is mentioned by
dbSNPrs141772938
ebirs141772938
HLIrs141772938
Exacrs141772938
Varsomers141772938
Maprs141772938
PheGenIrs141772938
hapmaprs141772938
1000 genomesrs141772938
hgdprs141772938
ensemblrs141772938
gopubmedrs141772938
geneviewrs141772938
scholarrs141772938
googlers141772938
pharmgkbrs141772938
gwascentralrs141772938
openSNPrs141772938
23andMers141772938
23andMe allrs141772938
SNP Nexus

SNPshotrs141772938
SNPdbers141772938
MSV3drs141772938
GWAS Ctlgrs141772938
Max Magnitude0
ClinVar
Risk rs141772938(G;G)
Alt rs141772938(G;G)
Reference rs141772938(C;C)
Significance Pathogenic
Disease Optic atrophy 9 not provided
Variation info
Gene ACO2
CLNDBN Optic atrophy 9 not provided
Reversed 0
HGVS NC_000022.10:g.41903841C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000169730.3, RCV000200405.2,