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rs797045170

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045170(G;T)
Make rs797045170(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161766447
GeneATF6, LOC102724329
is asnp
is mentioned by
dbSNPrs797045170
ebirs797045170
HLIrs797045170
Exacrs797045170
Varsomers797045170
Maprs797045170
PheGenIrs797045170
hapmaprs797045170
1000 genomesrs797045170
hgdprs797045170
ensemblrs797045170
gopubmedrs797045170
geneviewrs797045170
scholarrs797045170
googlers797045170
pharmgkbrs797045170
gwascentralrs797045170
openSNPrs797045170
23andMers797045170
23andMe allrs797045170
SNP Nexus

SNPshotrs797045170
SNPdbers797045170
MSV3drs797045170
GWAS Ctlgrs797045170
Max Magnitude0
ClinVar
Risk rs797045170(T;T)
Alt rs797045170(T;T)
Reference rs797045170(G;G)
Significance Pathogenic
Disease Achromatopsia 7
Variation info
Gene ATF6
CLNDBN Achromatopsia 7
Reversed 0
HGVS NC_000001.10:g.161736237G>T
CLNSRC
CLNACC RCV000191035.1,