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rs773881370

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs773881370(A;T)
Make rs773881370(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position15560607
GeneCC2D2A
is asnp
is mentioned by
dbSNPrs773881370
ebirs773881370
HLIrs773881370
Exacrs773881370
Varsomers773881370
Maprs773881370
PheGenIrs773881370
hapmaprs773881370
1000 genomesrs773881370
hgdprs773881370
ensemblrs773881370
gopubmedrs773881370
geneviewrs773881370
scholarrs773881370
googlers773881370
pharmgkbrs773881370
gwascentralrs773881370
openSNPrs773881370
23andMers773881370
23andMe allrs773881370
SNP Nexus

SNPshotrs773881370
SNPdbers773881370
MSV3drs773881370
GWAS Ctlgrs773881370
Max Magnitude0
ClinVar
Risk rs773881370(T;T)
Alt rs773881370(T;T)
Reference rs773881370(A;A)
Significance Pathogenic
Disease Joubert syndrome 9
Variation info
Gene CC2D2A
CLNDBN Joubert syndrome 9
Reversed 0
HGVS NC_000004.11:g.15562230A>T
CLNSRC
CLNACC RCV000201775.1,