rs6599175
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6599175(C;C) |
Make rs6599175(C;T) |
Make rs6599175(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 41744517 |
Gene | ULK4 |
is a | snp |
is | mentioned by |
dbSNP | rs6599175 |
dbSNP (classic) | rs6599175 |
ClinGen | rs6599175 |
ebi | rs6599175 |
HLI | rs6599175 |
Exac | rs6599175 |
Gnomad | rs6599175 |
Varsome | rs6599175 |
LitVar | rs6599175 |
Map | rs6599175 |
PheGenI | rs6599175 |
Biobank | rs6599175 |
1000 genomes | rs6599175 |
hgdp | rs6599175 |
ensembl | rs6599175 |
geneview | rs6599175 |
scholar | rs6599175 |
rs6599175 | |
pharmgkb | rs6599175 |
gwascentral | rs6599175 |
openSNP | rs6599175 |
23andMe | rs6599175 |
SNPshot | rs6599175 |
SNPdbe | rs6599175 |
MSV3d | rs6599175 |
GWAS Ctlg | rs6599175 |
GMAF | 0.2961 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23502783![]() |
Trait | Multiple myeloma (hyperdiploidy) |
Title | The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. |
Risk Allele | G |
P-val | 1E-9 |
Odds Ratio | 1.48 [1.30-1.68] |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 3
- 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 HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d