rs8061121
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs8061121(C;C) |
Make rs8061121(C;T) |
Make rs8061121(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 87159478 |
is a | snp |
is | mentioned by |
dbSNP | rs8061121 |
dbSNP (classic) | rs8061121 |
ClinGen | rs8061121 |
ebi | rs8061121 |
HLI | rs8061121 |
Exac | rs8061121 |
Gnomad | rs8061121 |
Varsome | rs8061121 |
LitVar | rs8061121 |
Map | rs8061121 |
PheGenI | rs8061121 |
Biobank | rs8061121 |
1000 genomes | rs8061121 |
hgdp | rs8061121 |
ensembl | rs8061121 |
geneview | rs8061121 |
scholar | rs8061121 |
rs8061121 | |
pharmgkb | rs8061121 |
gwascentral | rs8061121 |
openSNP | rs8061121 |
23andMe | rs8061121 |
SNPshot | rs8061121 |
SNPdbe | rs8061121 |
MSV3d | rs8061121 |
GWAS Ctlg | rs8061121 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 25138779] Genome-wide Association Study of Maternal and Inherited Effects on Left-Sided Cardiac Malformations