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rs863225169

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225169(C;C)
Make rs863225169(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position15567482
GeneCC2D2A
is asnp
is mentioned by
dbSNPrs863225169
ebirs863225169
HLIrs863225169
Exacrs863225169
Varsomers863225169
Maprs863225169
PheGenIrs863225169
hapmaprs863225169
1000 genomesrs863225169
hgdprs863225169
ensemblrs863225169
gopubmedrs863225169
geneviewrs863225169
scholarrs863225169
googlers863225169
pharmgkbrs863225169
gwascentralrs863225169
openSNPrs863225169
23andMers863225169
23andMe allrs863225169
SNP Nexus

SNPshotrs863225169
SNPdbers863225169
MSV3drs863225169
GWAS Ctlgrs863225169
Max Magnitude0
ClinVar
Risk rs863225169(C;C)
Alt rs863225169(C;C)
Reference rs863225169(G;G)
Significance Pathogenic
Disease Joubert syndrome 9
Variation info
Gene CC2D2A
CLNDBN Joubert syndrome 9
Reversed 0
HGVS NC_000004.11:g.15569105G>C
CLNSRC
CLNACC RCV000201720.1,