RS138587317 ALPL

Health Risk Chr 1:21563248

Upload your DNA to see your genotype for this variant.

What This Variant Does

"rs138587317, also known as c.436G&gt

Associated Conditions

Hypophosphatasia

Inborn genetic diseases

Adult hypophosphatasia

Childhood hypophosphatasia

Infantile hypophosphatasia

Hypophosphatasia

Inborn genetic diseases

Adult hypophosphatasia

Childhood hypophosphatasia

Infantile hypophosphatasia

Hypophosphatasia

GWAS Studies (3)

Trait	Risk Allele	OR / Beta	P-value	Study
Serum alkaline phosphatase levels	—	OR: 1.51	6E-174	PubMed
Serum alkaline phosphatase levels	—	OR: 1.71	4E-157	PubMed
Serum alkaline phosphatase levels	A	OR: 1.12	4E-110	PubMed

Other Variants in ALPL