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rs863225168

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225168(C;C)
Make rs863225168(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position15589654
GeneCC2D2A
is asnp
is mentioned by
dbSNPrs863225168
ebirs863225168
HLIrs863225168
Exacrs863225168
Varsomers863225168
Maprs863225168
PheGenIrs863225168
hapmaprs863225168
1000 genomesrs863225168
hgdprs863225168
ensemblrs863225168
gopubmedrs863225168
geneviewrs863225168
scholarrs863225168
googlers863225168
pharmgkbrs863225168
gwascentralrs863225168
openSNPrs863225168
23andMers863225168
23andMe allrs863225168
SNP Nexus

SNPshotrs863225168
SNPdbers863225168
MSV3drs863225168
GWAS Ctlgrs863225168
Max Magnitude0
ClinVar
Risk rs863225168(C;C)
Alt rs863225168(C;C)
Reference rs863225168(T;T)
Significance Pathogenic
Disease Joubert syndrome 9
Variation info
Gene CC2D2A
CLNDBN Joubert syndrome 9
Reversed 0
HGVS NC_000004.11:g.15591277T>C
CLNSRC
CLNACC RCV000201598.1,