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

rs587777140

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777140(-;-)
Make rs587777140(-;A)
ReferenceGRCh38 38.1/142
Chromosome8
Position67158500
GeneCSPP1
is asnp
is mentioned by
dbSNPrs587777140
ebirs587777140
HLIrs587777140
Exacrs587777140
Varsomers587777140
Maprs587777140
PheGenIrs587777140
hapmaprs587777140
1000 genomesrs587777140
hgdprs587777140
ensemblrs587777140
gopubmedrs587777140
geneviewrs587777140
scholarrs587777140
googlers587777140
pharmgkbrs587777140
gwascentralrs587777140
openSNPrs587777140
23andMers587777140
23andMe allrs587777140
SNP Nexus

SNPshotrs587777140
SNPdbers587777140
MSV3drs587777140
GWAS Ctlgrs587777140
Max Magnitude0
ClinVar
Risk rs587777140(;)
Alt rs587777140(;)
Reference rs587777140(A;A)
Significance Pathogenic
Disease Joubert syndrome 21
Variation info
Gene CSPP1
CLNDBN Joubert syndrome 21
Reversed 0
HGVS NC_000008.10:g.68070735delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000087068.6,