rs3773640
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3773640(A;A) |
Make rs3773640(A;T) |
Make rs3773640(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 3 |
Position | 30668019 |
Gene | TGFBR2 |
is a | snp |
is | mentioned by |
dbSNP | rs3773640 |
dbSNP (classic) | rs3773640 |
ClinGen | rs3773640 |
ebi | rs3773640 |
HLI | rs3773640 |
Exac | rs3773640 |
Gnomad | rs3773640 |
Varsome | rs3773640 |
LitVar | rs3773640 |
Map | rs3773640 |
PheGenI | rs3773640 |
Biobank | rs3773640 |
1000 genomes | rs3773640 |
hgdp | rs3773640 |
ensembl | rs3773640 |
geneview | rs3773640 |
scholar | rs3773640 |
rs3773640 | |
pharmgkb | rs3773640 |
gwascentral | rs3773640 |
openSNP | rs3773640 |
23andMe | rs3773640 |
SNPshot | rs3773640 |
SNPdbe | rs3773640 |
MSV3d | rs3773640 |
GWAS Ctlg | rs3773640 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 29580923] Endoglin pathway genetic variation in preeclampsia: A validation study in Norwegian and Latina cohorts.