RS775736341 SPART

Health Risk Chr 13:36335466
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What This Variant Does
"CLNSIG=5
Associated Conditions
Troyer syndrome
Inborn genetic diseases
Neurodevelopmental delay
Troyer syndrome
Inborn genetic diseases
Neurodevelopmental delay
Other Variants in SPART
rs1060499524 rs730882198 rs148833652 rs146398746 rs148399669 rs140222511 rs368305530 rs149730980 rs571222120 rs370385005
Ask Dr. Hemsworth about this variant