RS797044889 IQSEC2

Health Risk Chr X:53250523
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in IQSEC2
rs267607186 rs267607187 rs267607189 rs267607188 rs587777261 rs371450118 rs781940286 rs781805662 rs782536136 rs782748026
Ask Dr. Hemsworth about this variant