RS80356718 TARDBP

Health Risk Chr 1:11022209
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What This Variant Does
"CLNSIG=5
Associated Conditions
Amyotrophic lateral sclerosis type 10
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS
TARDBP-RELATED
TARDBP-related disorder
Inborn genetic diseases
Amyotrophic lateral sclerosis type 10
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS
TARDBP-RELATED
TARDBP-related disorder
Inborn genetic diseases
Other Variants in TARDBP
rs80356730 rs80356727 rs4884357 rs80356717 rs80356733 rs80356731 rs80356726 rs267607102 rs80356732 rs80356734
Ask Dr. Hemsworth about this variant