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rs779823379

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs779823379(A;A)
Make rs779823379(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position15580046
GeneCC2D2A
is asnp
is mentioned by
dbSNPrs779823379
ebirs779823379
HLIrs779823379
Exacrs779823379
Varsomers779823379
Maprs779823379
PheGenIrs779823379
hapmaprs779823379
1000 genomesrs779823379
hgdprs779823379
ensemblrs779823379
gopubmedrs779823379
geneviewrs779823379
scholarrs779823379
googlers779823379
pharmgkbrs779823379
gwascentralrs779823379
openSNPrs779823379
23andMers779823379
23andMe allrs779823379
SNP Nexus

SNPshotrs779823379
SNPdbers779823379
MSV3drs779823379
GWAS Ctlgrs779823379
Max Magnitude0
ClinVar
Risk rs779823379(A,T;A,T)
Alt rs779823379(A,T;A,T)
Reference rs779823379(C;C)
Significance Pathogenic
Disease Joubert syndrome 9
Variation info
Gene CC2D2A
CLNDBN Joubert syndrome 9
Reversed 0
HGVS NC_000004.11:g.15581669C>T
CLNSRC
CLNACC RCV000201552.1,