RS869312968 AIMP2

Health Risk Chr 7:6023301
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Leukodystrophy
hypomyelinating
17
Inborn genetic diseases
Leukodystrophy
hypomyelinating
17
Other Variants in AIMP2
rs529613640 rs760123492 rs147658637 rs1786357576 rs1786358808 rs140850823
Ask Dr. Hemsworth about this variant