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rs863224884

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224884(A;A)
Make rs863224884(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position232770905
GeneGIGYF2, KCNJ13
is asnp
is mentioned by
dbSNPrs863224884
ebirs863224884
HLIrs863224884
Exacrs863224884
Varsomers863224884
Maprs863224884
PheGenIrs863224884
hapmaprs863224884
1000 genomesrs863224884
hgdprs863224884
ensemblrs863224884
gopubmedrs863224884
geneviewrs863224884
scholarrs863224884
googlers863224884
pharmgkbrs863224884
gwascentralrs863224884
openSNPrs863224884
23andMers863224884
23andMe allrs863224884
SNP Nexus

SNPshotrs863224884
SNPdbers863224884
MSV3drs863224884
GWAS Ctlgrs863224884
Max Magnitude0
ClinVar
Risk rs863224884(A;A)
Alt rs863224884(A;A)
Reference rs863224884(G;G)
Significance Probable-Pathogenic
Disease Leber congenital amaurosis 16
Variation info
Gene GIGYF2 LOC101928854 KCNJ13
CLNDBN Leber congenital amaurosis 16
Reversed 0
HGVS NC_000002.11:g.233635615G>A
CLNSRC
CLNACC RCV000197888.1,