rs1264308
From SNPedia
Orientation | minus |
Make rs1264308(A;A) |
Make rs1264308(A;G) |
Make rs1264308(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 6 |
Position | 30912210 |
Gene | GTF2H4, VARS2 |
is a | snp |
is | mentioned by |
dbSNP | rs1264308 |
dbSNP (classic) | rs1264308 |
ClinGen | rs1264308 |
ebi | rs1264308 |
HLI | rs1264308 |
Exac | rs1264308 |
Gnomad | rs1264308 |
Varsome | rs1264308 |
LitVar | rs1264308 |
Map | rs1264308 |
PheGenI | rs1264308 |
Biobank | rs1264308 |
1000 genomes | rs1264308 |
hgdp | rs1264308 |
ensembl | rs1264308 |
geneview | rs1264308 |
scholar | rs1264308 |
rs1264308 | |
pharmgkb | rs1264308 |
gwascentral | rs1264308 |
openSNP | rs1264308 |
23andMe | rs1264308 |
SNPshot | rs1264308 |
SNPdbe | rs1264308 |
MSV3d | rs1264308 |
GWAS Ctlg | rs1264308 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 31026346] Genetic variants of genes in the NER pathway associated with risk of breast cancer: a large-scale analysis of 14 published GWAS datasets in the DRIVE Study.