RS4399848 Unknown gene
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What This Variant Does
"SNP rs4399848 (Chr 3 at 28.679467 Mb, band 3p24.1, dbSNP build 128) is associated weakly with hypert..."
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Core binding factor acute myeloid leukemia | A | — | 9E-6 | PubMed |