rs34354770
From SNPedia
Orientation | plus |
Make rs34354770(A;A) |
Make rs34354770(A;C) |
Make rs34354770(C;C) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 13 |
Position | 23753479 |
Gene | MIPEP |
is a | snp |
is | mentioned by |
dbSNP | rs34354770 |
dbSNP (classic) | rs34354770 |
ClinGen | rs34354770 |
ebi | rs34354770 |
HLI | rs34354770 |
Exac | rs34354770 |
Gnomad | rs34354770 |
Varsome | rs34354770 |
LitVar | rs34354770 |
Map | rs34354770 |
PheGenI | rs34354770 |
Biobank | rs34354770 |
1000 genomes | rs34354770 |
hgdp | rs34354770 |
ensembl | rs34354770 |
geneview | rs34354770 |
scholar | rs34354770 |
rs34354770 | |
pharmgkb | rs34354770 |
gwascentral | rs34354770 |
openSNP | rs34354770 |
23andMe | rs34354770 |
SNPshot | rs34354770 |
SNPdbe | rs34354770 |
MSV3d | rs34354770 |
GWAS Ctlg | rs34354770 |
Max Magnitude | 0 |
[PMID 31126313] The inherited variations of a p53-responsive enhancer in 13q12.12 confer lung cancer risk by attenuating TNFRSF19 expression.