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rs141153181

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs141153181(G;T)
Make rs141153181(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position37198775
GeneC5orf42
is asnp
is mentioned by
dbSNPrs141153181
ebirs141153181
HLIrs141153181
Exacrs141153181
Varsomers141153181
Maprs141153181
PheGenIrs141153181
hapmaprs141153181
1000 genomesrs141153181
hgdprs141153181
ensemblrs141153181
gopubmedrs141153181
geneviewrs141153181
scholarrs141153181
googlers141153181
pharmgkbrs141153181
gwascentralrs141153181
openSNPrs141153181
23andMers141153181
23andMe allrs141153181
SNP Nexus

SNPshotrs141153181
SNPdbers141153181
MSV3drs141153181
GWAS Ctlgrs141153181
Max Magnitude0
ClinVar
Risk rs141153181(A,T;A,T)
Alt rs141153181(A,T;A,T)
Reference rs141153181(G;G)
Significance Pathogenic
Disease Joubert syndrome 17
Variation info
Gene C5orf42
CLNDBN Joubert syndrome 17
Reversed 0
HGVS NC_000005.9:g.37198877G>A
CLNSRC
CLNACC RCV000201619.1,