rs4248154
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs4248154(C;T) |
Make rs4248154(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31034839 |
Gene | MUC22 |
is a | snp |
is | mentioned by |
dbSNP | rs4248154 |
dbSNP (classic) | rs4248154 |
ClinGen | rs4248154 |
ebi | rs4248154 |
HLI | rs4248154 |
Exac | rs4248154 |
Gnomad | rs4248154 |
Varsome | rs4248154 |
LitVar | rs4248154 |
Map | rs4248154 |
PheGenI | rs4248154 |
Biobank | rs4248154 |
1000 genomes | rs4248154 |
hgdp | rs4248154 |
ensembl | rs4248154 |
geneview | rs4248154 |
scholar | rs4248154 |
rs4248154 | |
pharmgkb | rs4248154 |
gwascentral | rs4248154 |
openSNP | rs4248154 |
23andMe | rs4248154 |
SNPshot | rs4248154 |
SNPdbe | rs4248154 |
MSV3d | rs4248154 |
GWAS Ctlg | rs4248154 |
GMAF | 0.2043 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21900946] |
Trait | |
Title | Identification of independent risk loci for Graves' disease within the MHC in the Japanese population. |
Risk Allele | C |
P-val | 1E-13 |
Odds Ratio | 1.3800 [1.27-1.50] |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 6
- 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