RS757332023 TIA1

Health Risk Chr 2:70212795
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What This Variant Does
"aka p.Pro362Leu or P362L The rare rs757332023(A) mutation was identified in a family with Amyotrophi..."
Associated Conditions
AMYOTROPHIC LATERAL SCLEROSIS 26 WITH FRONTOTEMPORAL DEMENTIA
Welander distal myopathy
AMYOTROPHIC LATERAL SCLEROSIS 26 WITH FRONTOTEMPORAL DEMENTIA
Welander distal myopathy
Other Variants in TIA1
rs747068278 rs116621885 rs201905164 rs200963371 rs767534980 rs769573516
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