rs2151280
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2151280(C;C) |
Make rs2151280(C;T) |
Make rs2151280(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 22034720 |
Gene | CDKN2B-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs2151280 |
dbSNP (classic) | rs2151280 |
ClinGen | rs2151280 |
ebi | rs2151280 |
HLI | rs2151280 |
Exac | rs2151280 |
Gnomad | rs2151280 |
Varsome | rs2151280 |
LitVar | rs2151280 |
Map | rs2151280 |
PheGenI | rs2151280 |
Biobank | rs2151280 |
1000 genomes | rs2151280 |
hgdp | rs2151280 |
ensembl | rs2151280 |
geneview | rs2151280 |
scholar | rs2151280 |
rs2151280 | |
pharmgkb | rs2151280 |
gwascentral | rs2151280 |
openSNP | rs2151280 |
23andMe | rs2151280 |
SNPshot | rs2151280 |
SNPdbe | rs2151280 |
MSV3d | rs2151280 |
GWAS Ctlg | rs2151280 |
GMAF | 0.4734 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
23andMe blog rs2151280 G 1.19 Basal Cell Carcinoma
[PMID 19578363] New common variants affecting susceptibility to basal cell carcinoma
[PMID 22034633] Role of Noncoding RNA ANRIL in Genesis of Plexiform Neurofibromas in Neurofibromatosis Type 1
GWAS snp | |
---|---|
PMID | [PMID 24403052] |
Trait | Basal cell carcinoma |
Title | Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma. |
Risk Allele | G |
P-val | 3E-10 |
Odds Ratio | 1.20 [1.14-1.27] |
[PMID 25874495] Long noncoding RNAs POLR2E rs3787016 C/T and HULC rs7763881 A/C polymorphisms are associated with decreased risk of esophageal cancer