RS587777011 FAM111A

Health Risk Chr 11:59153374
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What This Variant Does
"CLNSIG=255
Associated Conditions
Autosomal dominant Kenny-Caffey syndrome
Osteocraniostenosis
Inborn genetic diseases
Autosomal dominant Kenny-Caffey syndrome
Osteocraniostenosis
Inborn genetic diseases
Other Variants in FAM111A
rs2496296355 rs147361273 rs187676082 rs142539088 rs140306279 rs748812251 rs749677037 rs944930983 rs376721381 rs1298422871
Ask Dr. Hemsworth about this variant