rs34995925
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs34995925(C;C) |
Make rs34995925(C;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 88990213 |
Gene | ACTA2, FAS |
is a | snp |
is | mentioned by |
dbSNP | rs34995925 |
dbSNP (classic) | rs34995925 |
ClinGen | rs34995925 |
ebi | rs34995925 |
HLI | rs34995925 |
Exac | rs34995925 |
Gnomad | rs34995925 |
Varsome | rs34995925 |
LitVar | rs34995925 |
Map | rs34995925 |
PheGenI | rs34995925 |
Biobank | rs34995925 |
1000 genomes | rs34995925 |
hgdp | rs34995925 |
ensembl | rs34995925 |
geneview | rs34995925 |
scholar | rs34995925 |
rs34995925 | |
pharmgkb | rs34995925 |
gwascentral | rs34995925 |
openSNP | rs34995925 |
23andMe | rs34995925 |
SNPshot | rs34995925 |
SNPdbe | rs34995925 |
MSV3d | rs34995925 |
GWAS Ctlg | rs34995925 |
Max Magnitude | 0 |
[PMID 24448373] Association of specific diplotypes defined by common rs1800682 and rare rs34995925 single nucleotide polymorphisms within the STAT1 transcription binding site of the FAS gene promoter with preeclampsia