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rs13049286

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs13049286(G;G)
Make rs13049286(G;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position41756639
GeneRIPK4
is asnp
is mentioned by
dbSNPrs13049286
dbSNP (old)rs13049286
ClinGenrs13049286
ebirs13049286
HLIrs13049286
Exacrs13049286
Gnomadrs13049286
Varsomers13049286
Maprs13049286
PheGenIrs13049286
Biobankrs13049286
1000 genomesrs13049286
hgdprs13049286
ensemblrs13049286
gopubmedrs13049286
geneviewrs13049286
scholarrs13049286
googlers13049286
pharmgkbrs13049286
gwascentralrs13049286
openSNPrs13049286
23andMers13049286
23andMe allrs13049286
SNP Nexus

SNPshotrs13049286
SNPdbers13049286
MSV3drs13049286
GWAS Ctlgrs13049286
GMAF0.1116
Max Magnitude0
? (G;G) (G;T) (T;T) 28
[PMID 22479419OA-icon.png] Genome-wide association study of treatment refractory schizophrenia in han chinese


ClinVar
Risk rs13049286(G;G)
Alt rs13049286(G;G)
Reference Rs13049286(T;T)
Significance Probable-non-pathogenic
Disease Popliteal pterygium syndrome
Variation info
Gene RIPK4
CLNDBN Popliteal pterygium syndrome
Reversed 0
HGVS NC_000021.8:g.43176799T>G
CLNSRC
CLNACC RCV000317325.1,