RS398122523 ARFGEF2

Health Risk Chr 20:48976200
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What This Variant Does
"CLNSIG=5
Associated Conditions
Periventricular heterotopia with microcephaly
autosomal recessive
Periventricular heterotopia with microcephaly
autosomal recessive
Other Variants in ARFGEF2
rs28937880 rs147617265 rs117131028 rs538199862 rs147534008 rs73113975 rs200945599 rs187176143 rs61748373 rs151221957
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