rs3741206
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3741206(A;A) |
Make rs3741206(A;G) |
Make rs3741206(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 11 |
Position | 2148634 |
Gene | IGF2, IGF2-AS, INS-IGF2 |
is a | snp |
is | mentioned by |
dbSNP | rs3741206 |
dbSNP (classic) | rs3741206 |
ClinGen | rs3741206 |
ebi | rs3741206 |
HLI | rs3741206 |
Exac | rs3741206 |
Gnomad | rs3741206 |
Varsome | rs3741206 |
LitVar | rs3741206 |
Map | rs3741206 |
PheGenI | rs3741206 |
Biobank | rs3741206 |
1000 genomes | rs3741206 |
hgdp | rs3741206 |
ensembl | rs3741206 |
geneview | rs3741206 |
scholar | rs3741206 |
rs3741206 | |
pharmgkb | rs3741206 |
gwascentral | rs3741206 |
openSNP | rs3741206 |
23andMe | rs3741206 |
SNPshot | rs3741206 |
SNPdbe | rs3741206 |
MSV3d | rs3741206 |
GWAS Ctlg | rs3741206 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 28443481] Impact of Abnormal DNA Methylation of Imprinted Loci on Human Spontaneous Abortion.