RS770185023 IFT140

Health Risk Chr 16:1586276
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What This Variant Does
"CLNSIG=5
Associated Conditions
Jeune thoracic dystrophy
Saldino-Mainzer syndrome
Retinitis pigmentosa 80
Retinitis pigmentosa
Inborn genetic diseases
Acute myeloid leukemia
Jeune thoracic dystrophy
Saldino-Mainzer syndrome
Retinitis pigmentosa 80
Retinitis pigmentosa
Inborn genetic diseases
Acute myeloid leukemia
Other Variants in IFT140
rs387907192 rs376586707 rs387907193 rs431905506 rs201188361 rs587776909 rs431905520 rs431905521 rs199826737 rs431905522
Ask Dr. Hemsworth about this variant