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rs863225153

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225153(G;T)
Make rs863225153(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position37125324
GeneC5orf42
is asnp
is mentioned by
dbSNPrs863225153
ebirs863225153
HLIrs863225153
Exacrs863225153
Varsomers863225153
Maprs863225153
PheGenIrs863225153
hapmaprs863225153
1000 genomesrs863225153
hgdprs863225153
ensemblrs863225153
gopubmedrs863225153
geneviewrs863225153
scholarrs863225153
googlers863225153
pharmgkbrs863225153
gwascentralrs863225153
openSNPrs863225153
23andMers863225153
23andMe allrs863225153
SNP Nexus

SNPshotrs863225153
SNPdbers863225153
MSV3drs863225153
GWAS Ctlgrs863225153
Max Magnitude0
ClinVar
Risk rs863225153(T;T)
Alt rs863225153(T;T)
Reference rs863225153(G;G)
Significance Pathogenic
Disease Joubert syndrome 17
Variation info
Gene C5orf42
CLNDBN Joubert syndrome 17
Reversed 1
HGVS NC_000005.9:g.37125426C>A
CLNSRC
CLNACC RCV000201530.1,