rs374644
From SNPedia
Merged into | rs360064 |
Orientation | plus |
Make rs374644(G;G) |
Make rs374644(G;T) |
Make rs374644(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 1 |
Position | 225918985 |
is a | snp |
is | mentioned by |
dbSNP | rs374644 |
dbSNP (classic) | rs374644 |
ClinGen | rs374644 |
ebi | rs374644 |
HLI | rs374644 |
Exac | rs374644 |
Gnomad | rs374644 |
Varsome | rs374644 |
LitVar | rs374644 |
Map | rs374644 |
PheGenI | rs374644 |
Biobank | rs374644 |
1000 genomes | rs374644 |
hgdp | rs374644 |
ensembl | rs374644 |
geneview | rs374644 |
scholar | rs374644 |
rs374644 | |
pharmgkb | rs374644 |
gwascentral | rs374644 |
openSNP | rs374644 |
23andMe | rs374644 |
SNPshot | rs374644 |
SNPdbe | rs374644 |
MSV3d | rs374644 |
GWAS Ctlg | rs374644 |
Status | Merged into rs360064 |
Max Magnitude | 0 |
[PMID 30084801] Association of a MiR-499 SNP and risk of congenital heart disease in a Chinese population.