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rs863225174

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225174(A;G)
Make rs863225174(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position15601303
GeneCC2D2A
is asnp
is mentioned by
dbSNPrs863225174
ebirs863225174
HLIrs863225174
Exacrs863225174
Varsomers863225174
Maprs863225174
PheGenIrs863225174
hapmaprs863225174
1000 genomesrs863225174
hgdprs863225174
ensemblrs863225174
gopubmedrs863225174
geneviewrs863225174
scholarrs863225174
googlers863225174
pharmgkbrs863225174
gwascentralrs863225174
openSNPrs863225174
23andMers863225174
23andMe allrs863225174
SNP Nexus

SNPshotrs863225174
SNPdbers863225174
MSV3drs863225174
GWAS Ctlgrs863225174
Max Magnitude0
ClinVar
Risk rs863225174(G;G)
Alt rs863225174(G;G)
Reference rs863225174(A;A)
Significance Pathogenic
Disease Joubert syndrome 9
Variation info
Gene CC2D2A
CLNDBN Joubert syndrome 9
Reversed 0
HGVS NC_000004.11:g.15602926A>G
CLNSRC
CLNACC RCV000201684.1,