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rs587777809

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777809(A;G)
Make rs587777809(G;G)
ReferenceGRCh38 38.1/142
Chromosome14
Position88833691
GeneTTC8
is asnp
is mentioned by
dbSNPrs587777809
ebirs587777809
HLIrs587777809
Exacrs587777809
Varsomers587777809
Maprs587777809
PheGenIrs587777809
hapmaprs587777809
1000 genomesrs587777809
hgdprs587777809
ensemblrs587777809
gopubmedrs587777809
geneviewrs587777809
scholarrs587777809
googlers587777809
pharmgkbrs587777809
gwascentralrs587777809
openSNPrs587777809
23andMers587777809
23andMe allrs587777809
SNP Nexus

SNPshotrs587777809
SNPdbers587777809
MSV3drs587777809
GWAS Ctlgrs587777809
Max Magnitude0
ClinVar
Risk rs587777809(G;G)
Alt rs587777809(G;G)
Reference rs587777809(A;A)
Significance Pathogenic
Disease Retinitis pigmentosa 51
Variation info
Gene TTC8
CLNDBN Retinitis pigmentosa 51
Reversed 0
HGVS NC_000014.8:g.89300035A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000002641.5,