RS80293130 NRXN1

Health Risk Chr 2:50506533
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Associated Conditions
Chromosome 2p16.3 deletion syndrome
Pitt-Hopkins-like syndrome 2
Inborn genetic diseases
Chromosome 2p16.3 deletion syndrome
Pitt-Hopkins-like syndrome 2
Inborn genetic diseases
Other Variants in NRXN1
rs267606922 rs1558507406 rs55640811 rs113028018 rs372311299 rs201818223 rs192909520 rs200468214 rs201118246 rs75137449
Ask Dr. Hemsworth about this variant