rs28936407
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs28936407(A;A) |
Make rs28936407(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 12416831 |
Gene | PPARG |
is a | snp |
is | mentioned by |
dbSNP | rs28936407 |
dbSNP (classic) | rs28936407 |
ClinGen | rs28936407 |
ebi | rs28936407 |
HLI | rs28936407 |
Exac | rs28936407 |
Gnomad | rs28936407 |
Varsome | rs28936407 |
LitVar | rs28936407 |
Map | rs28936407 |
PheGenI | rs28936407 |
Biobank | rs28936407 |
1000 genomes | rs28936407 |
hgdp | rs28936407 |
ensembl | rs28936407 |
geneview | rs28936407 |
scholar | rs28936407 |
rs28936407 | |
pharmgkb | rs28936407 |
gwascentral | rs28936407 |
openSNP | rs28936407 |
23andMe | rs28936407 |
SNPshot | rs28936407 |
SNPdbe | rs28936407 |
MSV3d | rs28936407 |
GWAS Ctlg | rs28936407 |
Max Magnitude | 0 |
NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP
ClinVar | |
---|---|
Risk | rs28936407(A;A) |
Alt | rs28936407(A;A) |
Reference | Rs28936407(G;G) |
Significance | Pathogenic |
Disease | Carcinoma of colon |
Variation | info |
Gene | PPARG |
CLNDBN | Carcinoma of colon |
Reversed | 0 |
HGVS | NC_000003.11:g.12458330G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000008611.4, |