rs6550005
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6550005(A;A) |
Make rs6550005(A;G) |
Make rs6550005(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 3 |
Position | 30608572 |
Gene | TGFBR2 |
is a | snp |
is | mentioned by |
dbSNP | rs6550005 |
dbSNP (classic) | rs6550005 |
ClinGen | rs6550005 |
ebi | rs6550005 |
HLI | rs6550005 |
Exac | rs6550005 |
Gnomad | rs6550005 |
Varsome | rs6550005 |
LitVar | rs6550005 |
Map | rs6550005 |
PheGenI | rs6550005 |
Biobank | rs6550005 |
1000 genomes | rs6550005 |
hgdp | rs6550005 |
ensembl | rs6550005 |
geneview | rs6550005 |
scholar | rs6550005 |
rs6550005 | |
pharmgkb | rs6550005 |
gwascentral | rs6550005 |
openSNP | rs6550005 |
23andMe | rs6550005 |
SNPshot | rs6550005 |
SNPdbe | rs6550005 |
MSV3d | rs6550005 |
GWAS Ctlg | rs6550005 |
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.
[PMID 29183791] Transforming growth factor beta 1 related gene polymorphisms in gestational hypertension and preeclampsia: A case-control candidate gene association study.