RS121909762 ADGRV1

Health Risk Chr 5:90690991
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What This Variant Does
"[OMIM:?]
Associated Conditions
Usher syndrome type 2C
Usher syndrome
Febrile seizures
familial
4
Rare genetic deafness
Usher syndrome type 2C
Usher syndrome
Febrile seizures
familial
4
Rare genetic deafness
Other Variants in ADGRV1
rs121909761 rs796051863 rs796051864 rs796051865 rs121909763 rs796051866 rs796051867 rs1554135663 rs397517418 rs113938044
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