rs121909242
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs121909242(A;C) |
Make rs121909242(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 12416825 |
Gene | PPARG |
is a | snp |
is | mentioned by |
dbSNP | rs121909242 |
dbSNP (classic) | rs121909242 |
ClinGen | rs121909242 |
ebi | rs121909242 |
HLI | rs121909242 |
Exac | rs121909242 |
Gnomad | rs121909242 |
Varsome | rs121909242 |
LitVar | rs121909242 |
Map | rs121909242 |
PheGenI | rs121909242 |
Biobank | rs121909242 |
1000 genomes | rs121909242 |
hgdp | rs121909242 |
ensembl | rs121909242 |
geneview | rs121909242 |
scholar | rs121909242 |
rs121909242 | |
pharmgkb | rs121909242 |
gwascentral | rs121909242 |
openSNP | rs121909242 |
23andMe | rs121909242 |
SNPshot | rs121909242 |
SNPdbe | rs121909242 |
MSV3d | rs121909242 |
GWAS Ctlg | rs121909242 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121909242(C;C) |
Alt | rs121909242(C;C) |
Reference | Rs121909242(A;A) |
Significance | Pathogenic |
Disease | Carcinoma of colon |
Variation | info |
Gene | PPARG |
CLNDBN | Carcinoma of colon |
Reversed | 0 |
HGVS | NC_000003.11:g.12458324A>C |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000008609.4, |