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rs876661403

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661403(C;C)
Make rs876661403(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position88872452
GeneTTC8
is asnp
is mentioned by
dbSNPrs876661403
ebirs876661403
HLIrs876661403
Exacrs876661403
Varsomers876661403
Maprs876661403
PheGenIrs876661403
hapmaprs876661403
1000 genomesrs876661403
hgdprs876661403
ensemblrs876661403
gopubmedrs876661403
geneviewrs876661403
scholarrs876661403
googlers876661403
pharmgkbrs876661403
gwascentralrs876661403
openSNPrs876661403
23andMers876661403
23andMe allrs876661403
SNP Nexus

SNPshotrs876661403
SNPdbers876661403
MSV3drs876661403
GWAS Ctlgrs876661403
Max Magnitude0
ClinVar
Risk rs876661403(C;C)
Alt rs876661403(C;C)
Reference rs876661403(G;G)
Significance Pathogenic
Disease Retinitis pigmentosa 51
Variation info
Gene TTC8
CLNDBN Retinitis pigmentosa 51
Reversed 0
HGVS NC_000014.8:g.89338796G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000223936.1,