RS199960045 NRXN1

Health Risk Chr 2:51028004
Upload your DNA to see your genotype for this variant.
Associated Conditions
Pitt-Hopkins-like syndrome 2
Chromosome 2p16.3 deletion syndrome
See cases
Inborn genetic diseases
Pitt-Hopkins-like syndrome 2
Chromosome 2p16.3 deletion syndrome
See cases
Inborn genetic diseases
Other Variants in NRXN1
rs267606922 rs1558507406 rs55640811 rs113028018 rs372311299 rs201818223 rs192909520 rs200468214 rs201118246 rs75137449
Ask Dr. Hemsworth about this variant