rs4471514
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4471514(C;C) |
Make rs4471514(C;T) |
Make rs4471514(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 95273561 |
Gene | VEZT |
is a | snp |
is | mentioned by |
dbSNP | rs4471514 |
dbSNP (classic) | rs4471514 |
ClinGen | rs4471514 |
ebi | rs4471514 |
HLI | rs4471514 |
Exac | rs4471514 |
Gnomad | rs4471514 |
Varsome | rs4471514 |
LitVar | rs4471514 |
Map | rs4471514 |
PheGenI | rs4471514 |
Biobank | rs4471514 |
1000 genomes | rs4471514 |
hgdp | rs4471514 |
ensembl | rs4471514 |
geneview | rs4471514 |
scholar | rs4471514 |
rs4471514 | |
pharmgkb | rs4471514 |
gwascentral | rs4471514 |
openSNP | rs4471514 |
23andMe | rs4471514 |
SNPshot | rs4471514 |
SNPdbe | rs4471514 |
MSV3d | rs4471514 |
GWAS Ctlg | rs4471514 |
GMAF | 0.4651 |
Max Magnitude | 0 |
[PMID 22194441] Variants in KITLG predispose to testicular germ cell cancer independently from spermatogenic function