RS121918653 KITLG

Health Risk Chr 12:88545774
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What This Variant Does
"[OMIM:?]
Associated Conditions
Hyperpigmentation with or without hypopigmentation
familial progressive
Hyperpigmentation with or without hypopigmentation
familial progressive
Other Variants in KITLG
rs730882156 rs730882157 rs1057520539 rs1870699640 rs751013211 rs1404903521 rs2499184191 rs140316904 rs768146588 rs2499184366
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