RS2487305557 ERLIN2

Health Risk Chr 8:37744658
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Associated Conditions
Spastic paraplegia 18a
autosomal dominant
Spastic paraplegia 18a
autosomal dominant
Other Variants in ERLIN2
rs587776893 rs398123002 rs191003311 rs886041612 rs1057519172 rs745877709 rs763958615 rs112575270 rs778852699 rs1554517382
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