RS1006898944 WDR62

Health Risk Chr 19:36099453
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Associated Conditions
Inborn genetic diseases
Microcephaly 2
primary
autosomal recessive
with or without cortical malformations
Inborn genetic diseases
Microcephaly 2
primary
autosomal recessive
with or without cortical malformations
Other Variants in WDR62
rs397704721 rs267607176 rs267607177 rs397704725 rs387907082 rs587776899 rs387907083 rs587776900 rs587776901 rs387907084
Ask Dr. Hemsworth about this variant