RS1057518345 ADNP

Health Risk Chr 20:50894172
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder
Inborn genetic diseases
ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder
Other Variants in ADNP
rs587777522 rs587777523 rs587777524 rs587777525 rs587777526 rs1135401808 rs1555810376 rs886039649 rs886041116 rs886042001
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