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rs797045173

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045173(-;C)
Make rs797045173(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161802160
GeneATF6
is asnp
is mentioned by
dbSNPrs797045173
ClinGenrs797045173
ebirs797045173
HLIrs797045173
Exacrs797045173
Varsomers797045173
Maprs797045173
PheGenIrs797045173
hapmaprs797045173
1000 genomesrs797045173
hgdprs797045173
ensemblrs797045173
gopubmedrs797045173
geneviewrs797045173
scholarrs797045173
googlers797045173
pharmgkbrs797045173
gwascentralrs797045173
openSNPrs797045173
23andMers797045173
23andMe allrs797045173
SNP Nexus

SNPshotrs797045173
SNPdbers797045173
MSV3drs797045173
GWAS Ctlgrs797045173
Max Magnitude0
ClinVar
Risk rs797045173(C;C)
Alt rs797045173(C;C)
Reference Rs797045173(;)
Significance Pathogenic
Disease Achromatopsia 7
Variation info
Gene ATF6
CLNDBN Achromatopsia 7
Reversed 0
HGVS NC_000001.10:g.161771950dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000191039.2,