RS28756990 MLH3

Health Risk Chr 14:75047434 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
Colorectal cancer
hereditary nonpolyposis
type 7
Colorectal cancer
hereditary nonpolyposis
type 7
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Acylphosphatase-1 levels A OR: 1.91 2E-28 PubMed
Population Frequencies
gnomAD ALL
98.9%
1kG AFR
4.8%
1kG ALL
0.1%
1kG AMR
0.6%
1kG EAS
99%
1kG EUR
99.5%
1kG SAS
0.3%
Other Variants in MLH3
rs587776622 rs28939071 rs1431264077 rs377337763 rs797045117 rs201303087 rs28756987 rs55725216 rs144707485 rs370951929
Ask Dr. Hemsworth about this variant