rs4733220
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4733220(A;A) |
Make rs4733220(A;G) |
Make rs4733220(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 8 |
Position | 31043374 |
Gene | WRN |
is a | snp |
is | mentioned by |
dbSNP | rs4733220 |
dbSNP (classic) | rs4733220 |
ClinGen | rs4733220 |
ebi | rs4733220 |
HLI | rs4733220 |
Exac | rs4733220 |
Gnomad | rs4733220 |
Varsome | rs4733220 |
LitVar | rs4733220 |
Map | rs4733220 |
PheGenI | rs4733220 |
Biobank | rs4733220 |
1000 genomes | rs4733220 |
hgdp | rs4733220 |
ensembl | rs4733220 |
geneview | rs4733220 |
scholar | rs4733220 |
rs4733220 | |
pharmgkb | rs4733220 |
gwascentral | rs4733220 |
openSNP | rs4733220 |
23andMe | rs4733220 |
SNPshot | rs4733220 |
SNPdbe | rs4733220 |
MSV3d | rs4733220 |
GWAS Ctlg | rs4733220 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 29689049] Allelic interaction effects of DNA damage and repair genes on the predisposition to age-related cataract.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 8
- Has genotype
- Has population
- On chip 23andMe v3
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip Affy GenomeWide 6
- On chip 23andMe v1
- On chip 23andMe v2
- On chip FTDNA
- On chip FTDNA2
- On chip 23andMe v4
- On chip Ancestry v2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d