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

rs863225176

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225176(C;C)
Make rs863225176(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position15589591
GeneCC2D2A
is asnp
is mentioned by
dbSNPrs863225176
ebirs863225176
HLIrs863225176
Exacrs863225176
Varsomers863225176
Maprs863225176
PheGenIrs863225176
hapmaprs863225176
1000 genomesrs863225176
hgdprs863225176
ensemblrs863225176
gopubmedrs863225176
geneviewrs863225176
scholarrs863225176
googlers863225176
pharmgkbrs863225176
gwascentralrs863225176
openSNPrs863225176
23andMers863225176
23andMe allrs863225176
SNP Nexus

SNPshotrs863225176
SNPdbers863225176
MSV3drs863225176
GWAS Ctlgrs863225176
Max Magnitude0
ClinVar
Risk rs863225176(C;C)
Alt rs863225176(C;C)
Reference rs863225176(T;T)
Significance Pathogenic
Disease Joubert syndrome 9
Variation info
Gene CC2D2A
CLNDBN Joubert syndrome 9
Reversed 0
HGVS NC_000004.11:g.15591214T>C
CLNSRC
CLNACC RCV000201617.1,