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rs863225151

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225151(G;T)
Make rs863225151(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position74074252
GeneC2CD3
is asnp
is mentioned by
dbSNPrs863225151
ebirs863225151
HLIrs863225151
Exacrs863225151
Varsomers863225151
Maprs863225151
PheGenIrs863225151
hapmaprs863225151
1000 genomesrs863225151
hgdprs863225151
ensemblrs863225151
gopubmedrs863225151
geneviewrs863225151
scholarrs863225151
googlers863225151
pharmgkbrs863225151
gwascentralrs863225151
openSNPrs863225151
23andMers863225151
23andMe allrs863225151
SNP Nexus

SNPshotrs863225151
SNPdbers863225151
MSV3drs863225151
GWAS Ctlgrs863225151
Max Magnitude0
ClinVar
Risk rs863225151(T;T)
Alt rs863225151(T;T)
Reference rs863225151(G;G)
Significance Pathogenic
Disease Joubert syndrome
Variation info
Gene C2CD3
CLNDBN Joubert syndrome
Reversed 1
HGVS NC_000011.9:g.73785297C>A
CLNSRC
CLNACC RCV000201782.1,