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rs761129859

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs761129859(A;A)
Make rs761129859(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161821166
GeneATF6
is asnp
is mentioned by
dbSNPrs761129859
ebirs761129859
HLIrs761129859
Exacrs761129859
Varsomers761129859
Maprs761129859
PheGenIrs761129859
hapmaprs761129859
1000 genomesrs761129859
hgdprs761129859
ensemblrs761129859
gopubmedrs761129859
geneviewrs761129859
scholarrs761129859
googlers761129859
pharmgkbrs761129859
gwascentralrs761129859
openSNPrs761129859
23andMers761129859
23andMe allrs761129859
SNP Nexus

SNPshotrs761129859
SNPdbers761129859
MSV3drs761129859
GWAS Ctlgrs761129859
Max Magnitude0
ClinVar
Risk rs761129859(A;A)
Alt rs761129859(A;A)
Reference rs761129859(G;G)
Significance Pathogenic
Disease Achromatopsia 7
Variation info
Gene ATF6
CLNDBN Achromatopsia 7
Reversed 0
HGVS NC_000001.10:g.161790956G>C
CLNSRC
CLNACC RCV000191037.1,