rs10495098
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10495098(G;G) |
Make rs10495098(G;T) |
Make rs10495098(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 1 |
Position | 218342968 |
is a | snp |
is | mentioned by |
dbSNP | rs10495098 |
dbSNP (classic) | rs10495098 |
ClinGen | rs10495098 |
ebi | rs10495098 |
HLI | rs10495098 |
Exac | rs10495098 |
Gnomad | rs10495098 |
Varsome | rs10495098 |
LitVar | rs10495098 |
Map | rs10495098 |
PheGenI | rs10495098 |
Biobank | rs10495098 |
1000 genomes | rs10495098 |
hgdp | rs10495098 |
ensembl | rs10495098 |
geneview | rs10495098 |
scholar | rs10495098 |
rs10495098 | |
pharmgkb | rs10495098 |
gwascentral | rs10495098 |
openSNP | rs10495098 |
23andMe | rs10495098 |
SNPshot | rs10495098 |
SNPdbe | rs10495098 |
MSV3d | rs10495098 |
GWAS Ctlg | rs10495098 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 27564654] Genetic variance of transforming growth factor β2 gene in conotruncal heart defects.