Have questions? Visit https://www.reddit.com/r/SNPedia

rs794727531

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794727531(C;T)
Make rs794727531(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position94029555
GeneABCA4
is asnp
is mentioned by
dbSNPrs794727531
ebirs794727531
HLIrs794727531
Exacrs794727531
Varsomers794727531
Maprs794727531
PheGenIrs794727531
hapmaprs794727531
1000 genomesrs794727531
hgdprs794727531
ensemblrs794727531
gopubmedrs794727531
geneviewrs794727531
scholarrs794727531
googlers794727531
pharmgkbrs794727531
gwascentralrs794727531
openSNPrs794727531
23andMers794727531
23andMe allrs794727531
SNP Nexus

SNPshotrs794727531
SNPdbers794727531
MSV3drs794727531
GWAS Ctlgrs794727531
Max Magnitude0
ClinVar
Risk rs794727531(T;T)
Alt rs794727531(T;T)
Reference rs794727531(C;C)
Significance Pathogenic
Disease Stargardt disease 1
Variation info
Gene ABCA4
CLNDBN Stargardt disease 1
Reversed 1
HGVS NC_000001.10:g.94495111G>A
CLNSRC
CLNACC RCV000177441.1,