RS199784029 NRXN1

Health Risk Chr 2:51027952
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Associated Conditions
Pitt-Hopkins-like syndrome 2
Chromosome 2p16.3 deletion syndrome
Intellectual disability
Inborn genetic diseases
NRXN1-related disorder
Pitt-Hopkins-like syndrome 2
Chromosome 2p16.3 deletion syndrome
Intellectual disability
Inborn genetic diseases
NRXN1-related disorder
Other Variants in NRXN1
rs267606922 rs1558507406 rs55640811 rs113028018 rs372311299 rs201818223 rs192909520 rs200468214 rs201118246 rs75137449
Ask Dr. Hemsworth about this variant