rs1155708
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1155708(A;A) |
Make rs1155708(A;G) |
Make rs1155708(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 3 |
Position | 30645248 |
Gene | TGFBR2 |
is a | snp |
is | mentioned by |
dbSNP | rs1155708 |
dbSNP (classic) | rs1155708 |
ClinGen | rs1155708 |
ebi | rs1155708 |
HLI | rs1155708 |
Exac | rs1155708 |
Gnomad | rs1155708 |
Varsome | rs1155708 |
LitVar | rs1155708 |
Map | rs1155708 |
PheGenI | rs1155708 |
Biobank | rs1155708 |
1000 genomes | rs1155708 |
hgdp | rs1155708 |
ensembl | rs1155708 |
geneview | rs1155708 |
scholar | rs1155708 |
rs1155708 | |
pharmgkb | rs1155708 |
gwascentral | rs1155708 |
openSNP | rs1155708 |
23andMe | rs1155708 |
SNPshot | rs1155708 |
SNPdbe | rs1155708 |
MSV3d | rs1155708 |
GWAS Ctlg | rs1155708 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 29580923] Endoglin pathway genetic variation in preeclampsia: A validation study in Norwegian and Latina cohorts.