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rs763486732

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs763486732(A;A)
Make rs763486732(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position15586170
GeneCC2D2A
is asnp
is mentioned by
dbSNPrs763486732
ebirs763486732
HLIrs763486732
Exacrs763486732
Varsomers763486732
Maprs763486732
PheGenIrs763486732
hapmaprs763486732
1000 genomesrs763486732
hgdprs763486732
ensemblrs763486732
gopubmedrs763486732
geneviewrs763486732
scholarrs763486732
googlers763486732
pharmgkbrs763486732
gwascentralrs763486732
openSNPrs763486732
23andMers763486732
23andMe allrs763486732
SNP Nexus

SNPshotrs763486732
SNPdbers763486732
MSV3drs763486732
GWAS Ctlgrs763486732
Max Magnitude0
ClinVar
Risk rs763486732(A;A)
Alt rs763486732(A;A)
Reference rs763486732(G;G)
Significance Pathogenic
Disease Joubert syndrome 9
Variation info
Gene CC2D2A
CLNDBN Joubert syndrome 9
Reversed 0
HGVS NC_000004.11:g.15587793G>A
CLNSRC
CLNACC RCV000201714.1,