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rs863225178

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225178(A;A)
Make rs863225178(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position15557349
GeneCC2D2A
is asnp
is mentioned by
dbSNPrs863225178
ebirs863225178
HLIrs863225178
Exacrs863225178
Varsomers863225178
Maprs863225178
PheGenIrs863225178
hapmaprs863225178
1000 genomesrs863225178
hgdprs863225178
ensemblrs863225178
gopubmedrs863225178
geneviewrs863225178
scholarrs863225178
googlers863225178
pharmgkbrs863225178
gwascentralrs863225178
openSNPrs863225178
23andMers863225178
23andMe allrs863225178
SNP Nexus

SNPshotrs863225178
SNPdbers863225178
MSV3drs863225178
GWAS Ctlgrs863225178
Max Magnitude0
ClinVar
Risk rs863225178(A;A)
Alt rs863225178(A;A)
Reference rs863225178(G;G)
Significance Pathogenic
Disease Joubert syndrome 9
Variation info
Gene CC2D2A
CLNDBN Joubert syndrome 9
Reversed 0
HGVS NC_000004.11:g.15558972G>A
CLNSRC
CLNACC RCV000201758.1,