RS371981035 ADGRV1

Health Risk Chr 5:90810231
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rare genetic deafness
Retinal dystrophy
Usher syndrome type 2
Usher syndrome
Usher syndrome type 2C
Febrile seizures
familial
4
Rare genetic deafness
Retinal dystrophy
Usher syndrome type 2
Usher syndrome
Usher syndrome type 2C
Febrile seizures
familial
Other Variants in ADGRV1
rs121909761 rs121909762 rs796051863 rs796051864 rs796051865 rs121909763 rs796051866 rs796051867 rs1554135663 rs397517418
Ask Dr. Hemsworth about this variant