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rs760918829

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs760918829(C;C)
Make rs760918829(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position15574151
GeneCC2D2A
is asnp
is mentioned by
dbSNPrs760918829
ebirs760918829
HLIrs760918829
Exacrs760918829
Varsomers760918829
Maprs760918829
PheGenIrs760918829
hapmaprs760918829
1000 genomesrs760918829
hgdprs760918829
ensemblrs760918829
gopubmedrs760918829
geneviewrs760918829
scholarrs760918829
googlers760918829
pharmgkbrs760918829
gwascentralrs760918829
openSNPrs760918829
23andMers760918829
23andMe allrs760918829
SNP Nexus

SNPshotrs760918829
SNPdbers760918829
MSV3drs760918829
GWAS Ctlgrs760918829
Max Magnitude0
ClinVar
Risk rs760918829(C;C)
Alt rs760918829(C;C)
Reference rs760918829(T;T)
Significance Pathogenic
Disease Joubert syndrome 9
Variation info
Gene CC2D2A
CLNDBN Joubert syndrome 9
Reversed 0
HGVS NC_000004.11:g.15575774T>C
CLNSRC
CLNACC RCV000201761.1,