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

rs761188244

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs761188244(A;A)
Make rs761188244(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position94111370
GeneABCA4
is asnp
is mentioned by
dbSNPrs761188244
ebirs761188244
HLIrs761188244
Exacrs761188244
Varsomers761188244
Maprs761188244
PheGenIrs761188244
hapmaprs761188244
1000 genomesrs761188244
hgdprs761188244
ensemblrs761188244
gopubmedrs761188244
geneviewrs761188244
scholarrs761188244
googlers761188244
pharmgkbrs761188244
gwascentralrs761188244
openSNPrs761188244
23andMers761188244
23andMe allrs761188244
SNP Nexus

SNPshotrs761188244
SNPdbers761188244
MSV3drs761188244
GWAS Ctlgrs761188244
Max Magnitude0
ClinVar
Risk rs761188244(A;A)
Alt rs761188244(A;A)
Reference rs761188244(G;G)
Significance Probable-Pathogenic
Disease Stargardt disease 1
Variation info
Gene ABCA4
CLNDBN Stargardt disease 1
Reversed 0
HGVS NC_000001.10:g.94576926G>A
CLNSRC
CLNACC RCV000211040.1,