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