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rs587777805

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777805(C;T)
Make rs587777805(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position97784966
GeneARL6, LOC101929298
is asnp
is mentioned by
dbSNPrs587777805
ebirs587777805
HLIrs587777805
Exacrs587777805
Varsomers587777805
Maprs587777805
PheGenIrs587777805
hapmaprs587777805
1000 genomesrs587777805
hgdprs587777805
ensemblrs587777805
gopubmedrs587777805
geneviewrs587777805
scholarrs587777805
googlers587777805
pharmgkbrs587777805
gwascentralrs587777805
openSNPrs587777805
23andMers587777805
23andMe allrs587777805
SNP Nexus

SNPshotrs587777805
SNPdbers587777805
MSV3drs587777805
GWAS Ctlgrs587777805
Max Magnitude0
ClinVar
Risk rs587777805(G,T;G,T)
Alt rs587777805(G,T;G,T)
Reference rs587777805(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 55
Variation info
Gene ARL6 LOC101929298
CLNDBN Retinitis pigmentosa 55
Reversed 0
HGVS NC_000003.11:g.97503810C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002126.7,