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rs778858648

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs778858648(G;G)
Make rs778858648(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position15599632
GeneCC2D2A
is asnp
is mentioned by
dbSNPrs778858648
ebirs778858648
HLIrs778858648
Exacrs778858648
Varsomers778858648
Maprs778858648
PheGenIrs778858648
hapmaprs778858648
1000 genomesrs778858648
hgdprs778858648
ensemblrs778858648
gopubmedrs778858648
geneviewrs778858648
scholarrs778858648
googlers778858648
pharmgkbrs778858648
gwascentralrs778858648
openSNPrs778858648
23andMers778858648
23andMe allrs778858648
SNP Nexus

SNPshotrs778858648
SNPdbers778858648
MSV3drs778858648
GWAS Ctlgrs778858648
Max Magnitude0
ClinVar
Risk rs778858648(G;G)
Alt rs778858648(G;G)
Reference rs778858648(T;T)
Significance Pathogenic
Disease Joubert syndrome 9
Variation info
Gene CC2D2A
CLNDBN Joubert syndrome 9
Reversed 0
HGVS NC_000004.11:g.15601255T>G
CLNSRC
CLNACC RCV000201634.1,