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rs869320785

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869320785(C;T)
Make rs869320785(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position94027417
GeneABCA4
is asnp
is mentioned by
dbSNPrs869320785
ebirs869320785
HLIrs869320785
Exacrs869320785
Varsomers869320785
Maprs869320785
PheGenIrs869320785
hapmaprs869320785
1000 genomesrs869320785
hgdprs869320785
ensemblrs869320785
gopubmedrs869320785
geneviewrs869320785
scholarrs869320785
googlers869320785
pharmgkbrs869320785
gwascentralrs869320785
openSNPrs869320785
23andMers869320785
23andMe allrs869320785
SNP Nexus

SNPshotrs869320785
SNPdbers869320785
MSV3drs869320785
GWAS Ctlgrs869320785
Max Magnitude0
ClinVar
Risk rs869320785(T;T)
Alt rs869320785(T;T)
Reference rs869320785(C;C)
Significance Probable-Pathogenic
Disease Stargardt disease 1
Variation info
Gene ABCA4
CLNDBN Stargardt disease 1
Reversed 1
HGVS NC_000001.10:g.94492973G>A
CLNSRC
CLNACC RCV000211040.1,