RS1064794019 CERT1

Health Risk Chr 5:75426432
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What This Variant Does
"CLNSIG=5
Associated Conditions
Intellectual disability
autosomal dominant 34
Inborn genetic diseases
Intellectual disability
autosomal dominant 34
Inborn genetic diseases
Other Variants in CERT1
rs995534431 rs1057522045 rs1026933314 rs1554038957 rs1554039069 rs1554048616 rs1580752093 rs1763619016 rs1763618466 rs2112093130
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