RS1750497172 LMNB1

Health Risk Chr 5:126777605
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Associated Conditions
Syndrome with microcephaly as major feature
Microcephaly 26
primary
autosomal dominant
Inborn genetic diseases
Syndrome with microcephaly as major feature
Microcephaly 26
primary
autosomal dominant
Inborn genetic diseases
Other Variants in LMNB1
rs546757986 rs1750506249 rs757576125 rs190794874 rs372984423 rs370881377 rs138778484 rs368286117 rs2479520123 rs1751587092
Ask Dr. Hemsworth about this variant