rs1994198
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1994198(C;C) |
Make rs1994198(C;T) |
Make rs1994198(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 46360969 |
is a | snp |
is | mentioned by |
dbSNP | rs1994198 |
dbSNP (classic) | rs1994198 |
ClinGen | rs1994198 |
ebi | rs1994198 |
HLI | rs1994198 |
Exac | rs1994198 |
Gnomad | rs1994198 |
Varsome | rs1994198 |
LitVar | rs1994198 |
Map | rs1994198 |
PheGenI | rs1994198 |
Biobank | rs1994198 |
1000 genomes | rs1994198 |
hgdp | rs1994198 |
ensembl | rs1994198 |
geneview | rs1994198 |
scholar | rs1994198 |
rs1994198 | |
pharmgkb | rs1994198 |
gwascentral | rs1994198 |
openSNP | rs1994198 |
23andMe | rs1994198 |
SNPshot | rs1994198 |
SNPdbe | rs1994198 |
MSV3d | rs1994198 |
GWAS Ctlg | rs1994198 |
GMAF | 0.4146 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22130093] New variants at 10q26 and 15q21 are associated with aggressive prostate cancer in a genome-wide association study from a prostate biopsy screening cohort
[PMID 20514297] 2010 CUA Abstracts.