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rs116840813

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs116840813(A;G)
Make rs116840813(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position1440137
GeneRPS15
is asnp
is mentioned by
dbSNPrs116840813
ebirs116840813
HLIrs116840813
Exacrs116840813
Varsomers116840813
Maprs116840813
PheGenIrs116840813
hapmaprs116840813
1000 genomesrs116840813
hgdprs116840813
ensemblrs116840813
gopubmedrs116840813
geneviewrs116840813
scholarrs116840813
googlers116840813
pharmgkbrs116840813
gwascentralrs116840813
openSNPrs116840813
23andMers116840813
23andMe allrs116840813
SNP Nexus

SNPshotrs116840813
SNPdbers116840813
MSV3drs116840813
GWAS Ctlgrs116840813
Max Magnitude0
ClinVar
Risk rs116840813(G;G)
Alt rs116840813(G;G)
Reference rs116840813(A;A)
Significance Untested
Disease
Variation info
Gene RPS15
CLNDBN
Reversed 0
HGVS NC_000019.9:g.1440136A>G
CLNSRC
CLNACC