rs2667552
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2667552(C;C) |
Make rs2667552(C;T) |
Make rs2667552(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 78472009 |
Gene | WWOX |
is a | snp |
is | mentioned by |
dbSNP | rs2667552 |
dbSNP (classic) | rs2667552 |
ClinGen | rs2667552 |
ebi | rs2667552 |
HLI | rs2667552 |
Exac | rs2667552 |
Gnomad | rs2667552 |
Varsome | rs2667552 |
LitVar | rs2667552 |
Map | rs2667552 |
PheGenI | rs2667552 |
Biobank | rs2667552 |
1000 genomes | rs2667552 |
hgdp | rs2667552 |
ensembl | rs2667552 |
geneview | rs2667552 |
scholar | rs2667552 |
rs2667552 | |
pharmgkb | rs2667552 |
gwascentral | rs2667552 |
openSNP | rs2667552 |
23andMe | rs2667552 |
SNPshot | rs2667552 |
SNPdbe | rs2667552 |
MSV3d | rs2667552 |
GWAS Ctlg | rs2667552 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 28580594] Multiple single nucleotide polymorphism analysis and association of specific genotypes in FHIT, SAMD4A, and ANKRD17 in Indian patients with oral cancer.