RS773432002 ELP2

Health Risk Chr 18:36142309
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
ELP2-related disorder
Intellectual disability
autosomal recessive 58
Inborn genetic diseases
ELP2-related disorder
Intellectual disability
autosomal recessive 58
Other Variants in ELP2
rs1331690035 rs2511279303 rs780652067 rs2090721527 rs138742252 rs1403940898 rs553697188 rs529659464 rs2090515872 rs767713084
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