rs2272007
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs2272007(A;G) |
Make rs2272007(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 41954644 |
Gene | ULK4 |
is a | snp |
is | mentioned by |
dbSNP | rs2272007 |
dbSNP (classic) | rs2272007 |
ClinGen | rs2272007 |
ebi | rs2272007 |
HLI | rs2272007 |
Exac | rs2272007 |
Gnomad | rs2272007 |
Varsome | rs2272007 |
LitVar | rs2272007 |
Map | rs2272007 |
PheGenI | rs2272007 |
Biobank | rs2272007 |
1000 genomes | rs2272007 |
hgdp | rs2272007 |
ensembl | rs2272007 |
geneview | rs2272007 |
scholar | rs2272007 |
rs2272007 | |
pharmgkb | rs2272007 |
gwascentral | rs2272007 |
openSNP | rs2272007 |
23andMe | rs2272007 |
SNPshot | rs2272007 |
SNPdbe | rs2272007 |
MSV3d | rs2272007 |
GWAS Ctlg | rs2272007 |
GMAF | 0.3026 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | A |
P-val | 2E-9 |
Odds Ratio | 1.47 [1.30-1.67] |
ClinVar | |
---|---|
Risk | rs2272007(G;G) |
Alt | rs2272007(G;G) |
Reference | Rs2272007(A;A) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | ULK4 |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000003.11:g.41996136T>C |
CLNSRC | |
CLNACC | RCV000455513.1, |
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 FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d