rs2622604
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2622604(C;C) |
Make rs2622604(C;T) |
Make rs2622604(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 88157772 |
Gene | ABCG2 |
is a | snp |
is | mentioned by |
dbSNP | rs2622604 |
dbSNP (classic) | rs2622604 |
ClinGen | rs2622604 |
ebi | rs2622604 |
HLI | rs2622604 |
Exac | rs2622604 |
Gnomad | rs2622604 |
Varsome | rs2622604 |
LitVar | rs2622604 |
Map | rs2622604 |
PheGenI | rs2622604 |
Biobank | rs2622604 |
1000 genomes | rs2622604 |
hgdp | rs2622604 |
ensembl | rs2622604 |
geneview | rs2622604 |
scholar | rs2622604 |
rs2622604 | |
pharmgkb | rs2622604 |
gwascentral | rs2622604 |
openSNP | rs2622604 |
23andMe | rs2622604 |
SNPshot | rs2622604 |
SNPdbe | rs2622604 |
MSV3d | rs2622604 |
GWAS Ctlg | rs2622604 |
GMAF | 0.1832 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19696792] Single nucleotide polymorphism in ABCG2 is associated with irinotecan-induced severe myelosuppression
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 4
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d