RS199473693 ADAMTSL4

Health Risk Chr 1:150553750
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What This Variant Does
"CLNSIG=5
Associated Conditions
Ectopia lentis et pupillae
Ectopia lentis 2
isolated
autosomal recessive
Ectopia lentis
Craniosynostosis with ectopia lentis
Inborn genetic diseases
Ectopia lentis et pupillae
Ectopia lentis 2
isolated
autosomal recessive
Ectopia lentis
Craniosynostosis with ectopia lentis
Inborn genetic diseases
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Height — OR: 0.13 1E-12 PubMed
Other Variants in ADAMTSL4
rs118203985 rs587776927 rs794726688 rs368482584 rs794726689 rs747160538 rs112045022 rs56055939 rs202059899 rs115937511
Ask Dr. Hemsworth about this variant