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

rs368178632

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs368178632(A;G)
Make rs368178632(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position130416957
GeneCEP41
is asnp
is mentioned by
dbSNPrs368178632
ebirs368178632
HLIrs368178632
Exacrs368178632
Varsomers368178632
Maprs368178632
PheGenIrs368178632
hapmaprs368178632
1000 genomesrs368178632
hgdprs368178632
ensemblrs368178632
gopubmedrs368178632
geneviewrs368178632
scholarrs368178632
googlers368178632
pharmgkbrs368178632
gwascentralrs368178632
openSNPrs368178632
23andMers368178632
23andMe allrs368178632
SNP Nexus

SNPshotrs368178632
SNPdbers368178632
MSV3drs368178632
GWAS Ctlgrs368178632
Max Magnitude0
ClinVar
Risk rs368178632(G;G)
Alt rs368178632(G;G)
Reference rs368178632(A;A)
Significance Pathogenic
Disease Joubert syndrome 9/15
Variation info
Gene CEP41
CLNDBN Joubert syndrome 9/15, digenic
Reversed 0
HGVS NC_000007.13:g.130056798A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023827.2,