rs2229774
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common/normal |
(C;T) | 3 | higher risk for anthracycline side-effects for childhood cancer patients |
Make rs2229774(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 12 |
Position | 53211761 |
Gene | RARG |
is a | snp |
is | mentioned by |
dbSNP | rs2229774 |
dbSNP (classic) | rs2229774 |
ClinGen | rs2229774 |
ebi | rs2229774 |
HLI | rs2229774 |
Exac | rs2229774 |
Gnomad | rs2229774 |
Varsome | rs2229774 |
LitVar | rs2229774 |
Map | rs2229774 |
PheGenI | rs2229774 |
Biobank | rs2229774 |
1000 genomes | rs2229774 |
hgdp | rs2229774 |
ensembl | rs2229774 |
geneview | rs2229774 |
scholar | rs2229774 |
rs2229774 | |
pharmgkb | rs2229774 |
gwascentral | rs2229774 |
openSNP | rs2229774 |
23andMe | rs2229774 |
SNPshot | rs2229774 |
SNPdbe | rs2229774 |
MSV3d | rs2229774 |
GWAS Ctlg | rs2229774 |
Max Magnitude | 3 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
rs2229774, also known as p.Ser427Leu, in the RARG gene ups cardiotoxicity risk by roughly five times in children treated with the cancer drug anthracycline, based on a GWAS of a small number of anthracycline-treated childhood cancer patients (32 cases in the original discovery cohort and 22 in the replication population). The risk allele is the rare rs2229774(T) allele, in dbSNP orientation.10.1038/ng.3374
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 12
- Has genotype
- Has population
- Uses doi
- 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