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

rs61750641

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61750641(A;A)
Make rs61750641(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position94005499
GeneABCA4
is asnp
is mentioned by
dbSNPrs61750641
ebirs61750641
HLIrs61750641
Exacrs61750641
Varsomers61750641
Maprs61750641
PheGenIrs61750641
hapmaprs61750641
1000 genomesrs61750641
hgdprs61750641
ensemblrs61750641
gopubmedrs61750641
geneviewrs61750641
scholarrs61750641
googlers61750641
pharmgkbrs61750641
gwascentralrs61750641
openSNPrs61750641
23andMers61750641
23andMe allrs61750641
SNP Nexus

SNPshotrs61750641
SNPdbers61750641
MSV3drs61750641
GWAS Ctlgrs61750641
Max Magnitude0
ClinVar
Risk rs61750641(A;A)
Alt rs61750641(A;A)
Reference rs61750641(G;G)
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.94471055C>T
CLNSRC
CLNACC RCV000085787.1, RCV000178545.1,