RS886037834 PKD1L1

Health Risk Chr 7:47846960
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What This Variant Does
"CLNSIG=5
Associated Conditions
Situs inversus
Heterotaxy
visceral
8
autosomal
Inborn genetic diseases
Situs inversus
Heterotaxy
visceral
8
autosomal
Inborn genetic diseases
Other Variants in PKD1L1
rs528302390 rs116988549 rs111983425 rs10274334 rs139293796 rs147141584 rs150679968 rs145827073 rs142048596 rs144104914
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