RS528302390 PKD1L1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Situs inversus
Heterotaxy
visceral
8
autosomal
PKD1L1-related disorder
Inborn genetic diseases
Situs inversus
Heterotaxy
visceral
8
autosomal
PKD1L1-related disorder
Inborn genetic diseases
Other Variants in PKD1L1