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rs142513793

From SNPedia

Orientationplus
Stabilizedplus
Make rs142513793(C;C)
Make rs142513793(C;T)
Make rs142513793(T;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position48047088
is asnp
is mentioned by
dbSNPrs142513793
dbSNP (old)rs142513793
ClinGenrs142513793
ebirs142513793
HLIrs142513793
Exacrs142513793
Gnomadrs142513793
Varsomers142513793
Maprs142513793
PheGenIrs142513793
Biobankrs142513793
1000 genomesrs142513793
hgdprs142513793
ensemblrs142513793
gopubmedrs142513793
geneviewrs142513793
scholarrs142513793
googlers142513793
pharmgkbrs142513793
gwascentralrs142513793
openSNPrs142513793
23andMers142513793
23andMe allrs142513793
SNP Nexus

SNPshotrs142513793
SNPdbers142513793
MSV3drs142513793
GWAS Ctlgrs142513793
Max Magnitude
GWAS snp
PMID [PMID 24057671OA-icon.png]
Trait Tuberculosis
Title Genome-wide association study of ancestry-specific TB risk in the South African Coloured population.
Risk Allele C
P-val 2E-7
Odds Ratio 5.00 [NR]