rs12303082
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12303082(G;G) |
Make rs12303082(G;T) |
Make rs12303082(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 12 |
Position | 50360780 |
Gene | FAM186A |
is a | snp |
is | mentioned by |
dbSNP | rs12303082 |
dbSNP (classic) | rs12303082 |
ClinGen | rs12303082 |
ebi | rs12303082 |
HLI | rs12303082 |
Exac | rs12303082 |
Gnomad | rs12303082 |
Varsome | rs12303082 |
LitVar | rs12303082 |
Map | rs12303082 |
PheGenI | rs12303082 |
Biobank | rs12303082 |
1000 genomes | rs12303082 |
hgdp | rs12303082 |
ensembl | rs12303082 |
geneview | rs12303082 |
scholar | rs12303082 |
rs12303082 | |
pharmgkb | rs12303082 |
gwascentral | rs12303082 |
openSNP | rs12303082 |
23andMe | rs12303082 |
SNPshot | rs12303082 |
SNPdbe | rs12303082 |
MSV3d | rs12303082 |
GWAS Ctlg | rs12303082 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
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[PMID 26553438] Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer