rs3135974
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3135974(A;A) |
Make rs3135974(A;G) |
Make rs3135974(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 34988426 |
Gene | LIG3 |
is a | snp |
is | mentioned by |
dbSNP | rs3135974 |
dbSNP (classic) | rs3135974 |
ClinGen | rs3135974 |
ebi | rs3135974 |
HLI | rs3135974 |
Exac | rs3135974 |
Gnomad | rs3135974 |
Varsome | rs3135974 |
LitVar | rs3135974 |
Map | rs3135974 |
PheGenI | rs3135974 |
Biobank | rs3135974 |
1000 genomes | rs3135974 |
hgdp | rs3135974 |
ensembl | rs3135974 |
geneview | rs3135974 |
scholar | rs3135974 |
rs3135974 | |
pharmgkb | rs3135974 |
gwascentral | rs3135974 |
openSNP | rs3135974 |
23andMe | rs3135974 |
SNPshot | rs3135974 |
SNPdbe | rs3135974 |
MSV3d | rs3135974 |
GWAS Ctlg | rs3135974 |
GMAF | 0.0932 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20226869] Association between genetic variants in the base excision repair pathway and outcomes after hematopoietic cell transplants