RS118203963 SPG11

Health Risk Chr 15:44573651 snv stop gained
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What This Variant Does
"[OMIM:?]
Associated Conditions
Hereditary spastic paraplegia 11
Charcot-Marie-Tooth disease axonal type 2X
Inborn genetic diseases
Amyotrophic lateral sclerosis type 5
Hereditary spastic paraplegia 11
Charcot-Marie-Tooth disease axonal type 2X
Inborn genetic diseases
Amyotrophic lateral sclerosis type 5
Population Frequencies
gnomAD ALL
0%
Other Variants in SPG11
rs312262716 rs267607084 rs312262720 rs312262744 rs312262715 rs200079802 rs141848292 rs312262752 rs312262722 rs312262723
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