rs6478974
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6478974(A;A) |
Make rs6478974(A;T) |
Make rs6478974(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 9 |
Position | 99112121 |
Gene | TGFBR1 |
is a | snp |
is | mentioned by |
dbSNP | rs6478974 |
dbSNP (classic) | rs6478974 |
ClinGen | rs6478974 |
ebi | rs6478974 |
HLI | rs6478974 |
Exac | rs6478974 |
Gnomad | rs6478974 |
Varsome | rs6478974 |
LitVar | rs6478974 |
Map | rs6478974 |
PheGenI | rs6478974 |
Biobank | rs6478974 |
1000 genomes | rs6478974 |
hgdp | rs6478974 |
ensembl | rs6478974 |
geneview | rs6478974 |
scholar | rs6478974 |
rs6478974 | |
pharmgkb | rs6478974 |
gwascentral | rs6478974 |
openSNP | rs6478974 |
23andMe | rs6478974 |
SNPshot | rs6478974 |
SNPdbe | rs6478974 |
MSV3d | rs6478974 |
GWAS Ctlg | rs6478974 |
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.