rs2230949
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common genotype |
(G;G) | 0 |
Make rs2230949(C;T) |
Make rs2230949(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 11 |
Position | 2132958 |
Gene | IGF2, INS-IGF2 |
is a | snp |
is | mentioned by |
dbSNP | rs2230949 |
dbSNP (classic) | rs2230949 |
ClinGen | rs2230949 |
ebi | rs2230949 |
HLI | rs2230949 |
Exac | rs2230949 |
Gnomad | rs2230949 |
Varsome | rs2230949 |
LitVar | rs2230949 |
Map | rs2230949 |
PheGenI | rs2230949 |
Biobank | rs2230949 |
1000 genomes | rs2230949 |
hgdp | rs2230949 |
ensembl | rs2230949 |
geneview | rs2230949 |
scholar | rs2230949 |
rs2230949 | |
pharmgkb | rs2230949 |
gwascentral | rs2230949 |
openSNP | rs2230949 |
23andMe | rs2230949 |
SNPshot | rs2230949 |
SNPdbe | rs2230949 |
MSV3d | rs2230949 |
GWAS Ctlg | rs2230949 |
GMAF | 0.04867 |
Max Magnitude | 0 |
[PMID 18562769] Genetic variation in insulin-like growth factors and brain tumor risk.
[PMID 19936258] Epigenetic features of human mesenchymal stem cells determine their permissiveness for induction of relevant transcriptional changes by SYT-SSX1.