RS387907083 WDR62

Health Risk Chr 19:36083222
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What This Variant Does
"CLNSIG=5
Associated Conditions
Microcephaly 2
primary
autosomal recessive
with or without cortical malformations
Primary microcephaly type 2
Autosomal recessive primary microcephaly
Microcephaly 2
primary
autosomal recessive
with or without cortical malformations
Primary microcephaly type 2
Autosomal recessive primary microcephaly
Other Variants in WDR62
rs397704721 rs267607176 rs267607177 rs397704725 rs387907082 rs587776899 rs587776900 rs587776901 rs387907084 rs863223322
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