rs1607979
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1607979(A;A) |
Make rs1607979(A;G) |
Make rs1607979(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 53255898 |
is a | snp |
is | mentioned by |
dbSNP | rs1607979 |
dbSNP (classic) | rs1607979 |
ClinGen | rs1607979 |
ebi | rs1607979 |
HLI | rs1607979 |
Exac | rs1607979 |
Gnomad | rs1607979 |
Varsome | rs1607979 |
LitVar | rs1607979 |
Map | rs1607979 |
PheGenI | rs1607979 |
Biobank | rs1607979 |
1000 genomes | rs1607979 |
hgdp | rs1607979 |
ensembl | rs1607979 |
geneview | rs1607979 |
scholar | rs1607979 |
rs1607979 | |
pharmgkb | rs1607979 |
gwascentral | rs1607979 |
openSNP | rs1607979 |
23andMe | rs1607979 |
SNPshot | rs1607979 |
SNPdbe | rs1607979 |
MSV3d | rs1607979 |
GWAS Ctlg | rs1607979 |
GMAF | 0.4132 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24376627] How Genome-Wide SNP-SNP Interactions Relate to Nasopharyngeal Carcinoma Susceptibility