RS587776588 ENAM

Health Risk Chr 4:70642685
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What This Variant Does
"CLNSIG=255
Associated Conditions
Amelogenesis imperfecta type 1C
Amelogenesis imperfecta - hypoplastic autosomal dominant - local
ENAM-related disorder
Inborn genetic diseases
Amelogenesis imperfecta type 1C
Amelogenesis imperfecta - hypoplastic autosomal dominant - local
ENAM-related disorder
Inborn genetic diseases
Other Variants in ENAM
rs144225109 rs1738621357 rs1442845757 rs1738612312 rs2545343550 rs2109817825 rs138729240 rs148122591 rs775159311 rs373870116
Ask Dr. Hemsworth about this variant