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rs753955

From SNPedia

Orientationminus
Stabilizedminus
Make rs753955(C;C)
Make rs753955(C;T)
Make rs753955(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position23719720
GeneLOC105370113
is asnp
is mentioned by
dbSNPrs753955
dbSNP (classic)rs753955
ClinGenrs753955
ebirs753955
HLIrs753955
Exacrs753955
Gnomadrs753955
Varsomers753955
LitVarrs753955
Maprs753955
PheGenIrs753955
Biobankrs753955
1000 genomesrs753955
hgdprs753955
ensemblrs753955
geneviewrs753955
scholarrs753955
googlers753955
pharmgkbrs753955
gwascentralrs753955
openSNPrs753955
23andMers753955
SNPshotrs753955
SNPdbers753955
MSV3drs753955
GWAS Ctlgrs753955
GMAF0.4408
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 21725308]
Trait
Title A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese.
Risk Allele G
P-val 2E-12
Odds Ratio 1.1800 [1.13-1.24]


[PMID 31126313OA-icon.png] The inherited variations of a p53-responsive enhancer in 13q12.12 confer lung cancer risk by attenuating TNFRSF19 expression.