Have questions? Visit https://www.reddit.com/r/SNPedia

rs587777808

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777808(A;A)
Make rs587777808(A;G)
ReferenceGRCh38 38.1/142
Chromosome14
Position88843851
GeneTTC8
is asnp
is mentioned by
dbSNPrs587777808
ebirs587777808
HLIrs587777808
Exacrs587777808
Varsomers587777808
Maprs587777808
PheGenIrs587777808
hapmaprs587777808
1000 genomesrs587777808
hgdprs587777808
ensemblrs587777808
gopubmedrs587777808
geneviewrs587777808
scholarrs587777808
googlers587777808
pharmgkbrs587777808
gwascentralrs587777808
openSNPrs587777808
23andMers587777808
23andMe allrs587777808
SNP Nexus

SNPshotrs587777808
SNPdbers587777808
MSV3drs587777808
GWAS Ctlgrs587777808
Max Magnitude0
ClinVar
Risk rs587777808(A;A)
Alt rs587777808(A;A)
Reference rs587777808(G;G)
Significance Pathogenic
Disease Bardet-Biedl syndrome 8
Variation info
Gene TTC8
CLNDBN Bardet-Biedl syndrome 8
Reversed 0
HGVS NC_000014.8:g.89310195G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000002640.3,