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rs863225181

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225181(A;A)
Make rs863225181(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position15570501
GeneCC2D2A
is asnp
is mentioned by
dbSNPrs863225181
ebirs863225181
HLIrs863225181
Exacrs863225181
Varsomers863225181
Maprs863225181
PheGenIrs863225181
hapmaprs863225181
1000 genomesrs863225181
hgdprs863225181
ensemblrs863225181
gopubmedrs863225181
geneviewrs863225181
scholarrs863225181
googlers863225181
pharmgkbrs863225181
gwascentralrs863225181
openSNPrs863225181
23andMers863225181
23andMe allrs863225181
SNP Nexus

SNPshotrs863225181
SNPdbers863225181
MSV3drs863225181
GWAS Ctlgrs863225181
Max Magnitude0
ClinVar
Risk rs863225181(A;A)
Alt rs863225181(A;A)
Reference rs863225181(G;G)
Significance Probable-Pathogenic
Disease Joubert syndrome 9
Variation info
Gene CC2D2A
CLNDBN Joubert syndrome 9
Reversed 0
HGVS NC_000004.11:g.15572124G>A
CLNSRC
CLNACC RCV000201770.1,