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

rs61750120

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61750120(C;T)
Make rs61750120(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position94042767
GeneABCA4
is asnp
is mentioned by
dbSNPrs61750120
ebirs61750120
HLIrs61750120
Exacrs61750120
Varsomers61750120
Maprs61750120
PheGenIrs61750120
hapmaprs61750120
1000 genomesrs61750120
hgdprs61750120
ensemblrs61750120
gopubmedrs61750120
geneviewrs61750120
scholarrs61750120
googlers61750120
pharmgkbrs61750120
gwascentralrs61750120
openSNPrs61750120
23andMers61750120
23andMe allrs61750120
SNP Nexus

SNPshotrs61750120
SNPdbers61750120
MSV3drs61750120
GWAS Ctlgrs61750120
GMAF0.0004591
Max Magnitude0
ClinVar
Risk rs61750120(T;T)
Alt rs61750120(T;T)
Reference rs61750120(C;C)
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.94508323G>A
CLNSRC HGMD
CLNACC RCV000078665.3, RCV000150052.3,