RS137852944 PKHD1
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What This Variant Does
"rs137852944, also known as T36M or Thr36Met, is a SNP in the PKHD1 gene. It is the most common mutat...
Associated Conditions
Autosomal recessive polycystic kidney disease
Colorectal cancer
protection against
Polycystic kidney disease
Oligohydramnios
Periportal fibrosis
Autosomal dominant polycystic liver disease
Polycystic kidney disease 4
PKHD1-related disorder
See cases
Inborn genetic diseases
Renal cyst
Autosomal recessive polycystic kidney disease
Colorectal cancer
protection against
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Gamma glutamyl transferase levels | — | OR: 0.27 | 2E-12 | PubMed |
Other Variants in PKHD1