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rs797045174

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045174(-;A)
Make rs797045174(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161821084
GeneATF6
is asnp
is mentioned by
dbSNPrs797045174
ClinGenrs797045174
ebirs797045174
HLIrs797045174
Exacrs797045174
Varsomers797045174
Maprs797045174
PheGenIrs797045174
hapmaprs797045174
1000 genomesrs797045174
hgdprs797045174
ensemblrs797045174
gopubmedrs797045174
geneviewrs797045174
scholarrs797045174
googlers797045174
pharmgkbrs797045174
gwascentralrs797045174
openSNPrs797045174
23andMers797045174
23andMe allrs797045174
SNP Nexus

SNPshotrs797045174
SNPdbers797045174
MSV3drs797045174
GWAS Ctlgrs797045174
Max Magnitude0
ClinVar
Risk rs797045174(A;A)
Alt rs797045174(A;A)
Reference Rs797045174(;)
Significance Pathogenic
Disease Achromatopsia 7
Variation info
Gene ATF6
CLNDBN Achromatopsia 7
Reversed 0
HGVS NC_000001.10:g.161790874dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000191040.2,