rs1381392
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1381392(C;C) |
Make rs1381392(C;T) |
Make rs1381392(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 28707823 |
Gene | LINC00693 |
is a | snp |
is | mentioned by |
dbSNP | rs1381392 |
dbSNP (classic) | rs1381392 |
ClinGen | rs1381392 |
ebi | rs1381392 |
HLI | rs1381392 |
Exac | rs1381392 |
Gnomad | rs1381392 |
Varsome | rs1381392 |
LitVar | rs1381392 |
Map | rs1381392 |
PheGenI | rs1381392 |
Biobank | rs1381392 |
1000 genomes | rs1381392 |
hgdp | rs1381392 |
ensembl | rs1381392 |
geneview | rs1381392 |
scholar | rs1381392 |
rs1381392 | |
pharmgkb | rs1381392 |
gwascentral | rs1381392 |
openSNP | rs1381392 |
23andMe | rs1381392 |
SNPshot | rs1381392 |
SNPdbe | rs1381392 |
MSV3d | rs1381392 |
GWAS Ctlg | rs1381392 |
GMAF | 0.118 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24084763] Germline Variants and Advanced Colorectal Adenomas: Adenoma Prevention with Celecoxib Trial Genomewide Association Study
[PMID 19299336] Genome-wide association study to identify novel loci associated with therapy-related myeloid leukemia susceptibility.