Have questions? Visit https://www.reddit.com/r/SNPedia

rs576298659

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs576298659(C;T)
Make rs576298659(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position15586154
GeneCC2D2A
is asnp
is mentioned by
dbSNPrs576298659
ebirs576298659
HLIrs576298659
Exacrs576298659
Varsomers576298659
Maprs576298659
PheGenIrs576298659
hapmaprs576298659
1000 genomesrs576298659
hgdprs576298659
ensemblrs576298659
gopubmedrs576298659
geneviewrs576298659
scholarrs576298659
googlers576298659
pharmgkbrs576298659
gwascentralrs576298659
openSNPrs576298659
23andMers576298659
23andMe allrs576298659
SNP Nexus

SNPshotrs576298659
SNPdbers576298659
MSV3drs576298659
GWAS Ctlgrs576298659
Max Magnitude0
ClinVar
Risk rs576298659(A,T;A,T)
Alt rs576298659(A,T;A,T)
Reference rs576298659(C;C)
Significance Probable-Pathogenic
Disease Joubert syndrome 9
Variation info
Gene CC2D2A
CLNDBN Joubert syndrome 9
Reversed 0
HGVS NC_000004.11:g.15587777C>A
CLNSRC
CLNACC RCV000201676.1,