rs137854905
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
({{{allele1}}};{{{allele2}}}) | 0 | common in clinvar |
Make rs137854905(-;TGTTCTGAGAGTGATCACTCCAGAAAT) |
Make rs137854905(TGTTCTGAGAGTGATCACTCCAGAAAT;TGTTCTGAGAGTGATCACTCCAGAAAT) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 137198270 |
Gene | IFNGR1 |
is a | snp |
is | mentioned by |
dbSNP | rs137854905 |
dbSNP (classic) | rs137854905 |
ClinGen | rs137854905 |
ebi | rs137854905 |
HLI | rs137854905 |
Exac | rs137854905 |
Gnomad | rs137854905 |
Varsome | rs137854905 |
LitVar | rs137854905 |
Map | rs137854905 |
PheGenI | rs137854905 |
Biobank | rs137854905 |
1000 genomes | rs137854905 |
hgdp | rs137854905 |
ensembl | rs137854905 |
geneview | rs137854905 |
scholar | rs137854905 |
rs137854905 | |
pharmgkb | rs137854905 |
gwascentral | rs137854905 |
openSNP | rs137854905 |
23andMe | rs137854905 |
SNPshot | rs137854905 |
SNPdbe | rs137854905 |
MSV3d | rs137854905 |
GWAS Ctlg | rs137854905 |
Max Magnitude | 0 |
[PMID 24453034] Association study of SNPs of genes IFNGR1 (rs137854905), GSTT1 (rs71748309), and GSTP1 (rs1695) in gastric cancer development in samples of patient in the northern and northeastern Brazil
ClinVar | |
---|---|
Risk | rs137854905(TGTTCTGAGAGTGATCACTCCAGAAAT;TGTTCTGAGAGTGATCACTCCAGAAAT) |
Alt | rs137854905(TGTTCTGAGAGTGATCACTCCAGAAAT;TGTTCTGAGAGTGATCACTCCAGAAAT) |
Reference | Rs137854905(-;-) |
Significance | Untested |
Disease | not provided |
Variation | info |
Gene | IFNGR1 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000006.11:g.137519408_137519434dup27 |
CLNSRC | ClinVar |
CLNACC | RCV000097411.1, |