rs11129420
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11129420(A;A) |
Make rs11129420(A;T) |
Make rs11129420(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 3 |
Position | 30617049 |
Gene | TGFBR2 |
is a | snp |
is | mentioned by |
dbSNP | rs11129420 |
dbSNP (classic) | rs11129420 |
ClinGen | rs11129420 |
ebi | rs11129420 |
HLI | rs11129420 |
Exac | rs11129420 |
Gnomad | rs11129420 |
Varsome | rs11129420 |
LitVar | rs11129420 |
Map | rs11129420 |
PheGenI | rs11129420 |
Biobank | rs11129420 |
1000 genomes | rs11129420 |
hgdp | rs11129420 |
ensembl | rs11129420 |
geneview | rs11129420 |
scholar | rs11129420 |
rs11129420 | |
pharmgkb | rs11129420 |
gwascentral | rs11129420 |
openSNP | rs11129420 |
23andMe | rs11129420 |
SNPshot | rs11129420 |
SNPdbe | rs11129420 |
MSV3d | rs11129420 |
GWAS Ctlg | rs11129420 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
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[PMID 29580923] Endoglin pathway genetic variation in preeclampsia: A validation study in Norwegian and Latina cohorts.