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rs61751385

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs61751385(G;G)
Make rs61751385(G;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position94063110
GeneABCA4
is asnp
is mentioned by
dbSNPrs61751385
ebirs61751385
HLIrs61751385
Exacrs61751385
Varsomers61751385
Maprs61751385
PheGenIrs61751385
hapmaprs61751385
1000 genomesrs61751385
hgdprs61751385
ensemblrs61751385
gopubmedrs61751385
geneviewrs61751385
scholarrs61751385
googlers61751385
pharmgkbrs61751385
gwascentralrs61751385
openSNPrs61751385
23andMers61751385
23andMe allrs61751385
SNP Nexus

SNPshotrs61751385
SNPdbers61751385
MSV3drs61751385
GWAS Ctlgrs61751385
Max Magnitude0
ClinVar
Risk rs61751385(G;G)
Alt rs61751385(G;G)
Reference rs61751385(T;T)
Significance Pathogenic
Disease not provided Stargardt disease 1
Variation info
Gene ABCA4
CLNDBN not provided Stargardt disease 1
Reversed 1
HGVS NC_000001.10:g.94528666A>C
CLNSRC ClinVar Retina International
CLNACC RCV000085420.1, RCV000132587.1,