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rs794727903

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794727903(C;T)
Make rs794727903(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position94080697
GeneABCA4
is asnp
is mentioned by
dbSNPrs794727903
ebirs794727903
HLIrs794727903
Exacrs794727903
Varsomers794727903
Maprs794727903
PheGenIrs794727903
hapmaprs794727903
1000 genomesrs794727903
hgdprs794727903
ensemblrs794727903
gopubmedrs794727903
geneviewrs794727903
scholarrs794727903
googlers794727903
pharmgkbrs794727903
gwascentralrs794727903
openSNPrs794727903
23andMers794727903
23andMe allrs794727903
SNP Nexus

SNPshotrs794727903
SNPdbers794727903
MSV3drs794727903
GWAS Ctlgrs794727903
Max Magnitude0
ClinVar
Risk rs794727903(T;T)
Alt rs794727903(T;T)
Reference rs794727903(C;C)
Significance Pathogenic
Disease Stargardt disease 1 Cone-rod dystrophy 3
Variation info
Gene ABCA4
CLNDBN Stargardt disease 1 Cone-rod dystrophy 3
Reversed 1
HGVS NC_000001.10:g.94546253G>A
CLNSRC
CLNACC RCV000180146.1, RCV000180147.1,