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rs776886962

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs776886962(A;A)
Make rs776886962(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position37224655
GeneC5orf42
is asnp
is mentioned by
dbSNPrs776886962
ebirs776886962
HLIrs776886962
Exacrs776886962
Varsomers776886962
Maprs776886962
PheGenIrs776886962
hapmaprs776886962
1000 genomesrs776886962
hgdprs776886962
ensemblrs776886962
gopubmedrs776886962
geneviewrs776886962
scholarrs776886962
googlers776886962
pharmgkbrs776886962
gwascentralrs776886962
openSNPrs776886962
23andMers776886962
23andMe allrs776886962
SNP Nexus

SNPshotrs776886962
SNPdbers776886962
MSV3drs776886962
GWAS Ctlgrs776886962
Max Magnitude0
ClinVar
Risk rs776886962(A;A)
Alt rs776886962(A;A)
Reference rs776886962(G;G)
Significance Pathogenic
Disease Joubert syndrome 17
Variation info
Gene C5orf42
CLNDBN Joubert syndrome 17
Reversed 0
HGVS NC_000005.9:g.37224757G>A
CLNSRC
CLNACC RCV000201525.1,