RS587777036 PHC1

Health Risk Chr 12:8939418
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What This Variant Does
"CLNSIG=5
Associated Conditions
Microcephaly 11
primary
autosomal recessive
Primary microcephaly
Intellectual disability
Microcephaly 11
primary
autosomal recessive
Primary microcephaly
Intellectual disability
Other Variants in PHC1
rs2137054010
Ask Dr. Hemsworth about this variant