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rs863225179

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225179(A;C)
Make rs863225179(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position15597460
GeneCC2D2A
is asnp
is mentioned by
dbSNPrs863225179
ebirs863225179
HLIrs863225179
Exacrs863225179
Varsomers863225179
Maprs863225179
PheGenIrs863225179
hapmaprs863225179
1000 genomesrs863225179
hgdprs863225179
ensemblrs863225179
gopubmedrs863225179
geneviewrs863225179
scholarrs863225179
googlers863225179
pharmgkbrs863225179
gwascentralrs863225179
openSNPrs863225179
23andMers863225179
23andMe allrs863225179
SNP Nexus

SNPshotrs863225179
SNPdbers863225179
MSV3drs863225179
GWAS Ctlgrs863225179
Max Magnitude0
ClinVar
Risk rs863225179(C;C)
Alt rs863225179(C;C)
Reference Rs863225179(A;A)
Significance Pathogenic
Disease Joubert syndrome 9
Variation info
Gene CC2D2A
CLNDBN Joubert syndrome 9
Reversed 0
HGVS NC_000004.11:g.15599083A>C
CLNSRC
CLNACC RCV000201637.1,