RS397704725 WDR62

Health Risk Chr 19:36103666
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What This Variant Does
"CLNSIG=5
Associated Conditions
Microcephaly 2
primary
autosomal recessive
with or without cortical malformations
Microcephaly 2
primary
autosomal recessive
with or without cortical malformations
Other Variants in WDR62
rs397704721 rs267607176 rs267607177 rs387907082 rs587776899 rs387907083 rs587776900 rs587776901 rs387907084 rs863223322
Ask Dr. Hemsworth about this variant