RS386833967 CLN5

Health Risk Chr 13:77000845
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What This Variant Does
"rs386833967, also known as c.1103_1106delAACA and p.Lys368Serfs, represents a very rare deletion mut...
Associated Conditions
Neuronal ceroid lipofuscinosis 5
Neuronal ceroid lipofuscinosis
Neuronal ceroid lipofuscinosis 5
Neuronal ceroid lipofuscinosis
Other Variants in CLN5
rs386833969 rs104894385 rs28940280 rs104894386 rs121908292 rs267606738 rs148862100 rs1555274312 rs386833963 rs386833964
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