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rs61757484

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61757484(A;A)
Make rs61757484(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position6425489
GeneAIPL1
is asnp
is mentioned by
dbSNPrs61757484
ebirs61757484
HLIrs61757484
Exacrs61757484
Varsomers61757484
Maprs61757484
PheGenIrs61757484
hapmaprs61757484
1000 genomesrs61757484
hgdprs61757484
ensemblrs61757484
gopubmedrs61757484
geneviewrs61757484
scholarrs61757484
googlers61757484
pharmgkbrs61757484
gwascentralrs61757484
openSNPrs61757484
23andMers61757484
23andMe allrs61757484
SNP Nexus

SNPshotrs61757484
SNPdbers61757484
MSV3drs61757484
GWAS Ctlgrs61757484
Max Magnitude0
ClinVar
Risk rs61757484(A;A)
Alt rs61757484(A;A)
Reference rs61757484(G;G)
Significance Pathogenic
Disease Leber congenital amaurosis 4 not provided not specified
Variation info
Gene AIPL1
CLNDBN Leber congenital amaurosis 4 not provided not specified
Reversed 0
HGVS NC_000017.10:g.6328809G>A
CLNSRC ClinVar GeneReviews Retina International
CLNACC RCV000055938.1, RCV000086212.2, RCV000179481.1,