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rs863225170

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225170(C;C)
Make rs863225170(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position15569346
GeneCC2D2A
is asnp
is mentioned by
dbSNPrs863225170
ebirs863225170
HLIrs863225170
Exacrs863225170
Varsomers863225170
Maprs863225170
PheGenIrs863225170
hapmaprs863225170
1000 genomesrs863225170
hgdprs863225170
ensemblrs863225170
gopubmedrs863225170
geneviewrs863225170
scholarrs863225170
googlers863225170
pharmgkbrs863225170
gwascentralrs863225170
openSNPrs863225170
23andMers863225170
23andMe allrs863225170
SNP Nexus

SNPshotrs863225170
SNPdbers863225170
MSV3drs863225170
GWAS Ctlgrs863225170
Max Magnitude0
ClinVar
Risk rs863225170(C;C)
Alt rs863225170(C;C)
Reference rs863225170(T;T)
Significance Pathogenic
Disease Joubert syndrome 9
Variation info
Gene CC2D2A
CLNDBN Joubert syndrome 9
Reversed 0
HGVS NC_000004.11:g.15570969T>C
CLNSRC
CLNACC RCV000201640.1,