RS1021001959 NPRL3

Health Risk Chr 16:130572
Upload your DNA to see your genotype for this variant.
Associated Conditions
Epilepsy
familial focal
with variable foci 3
Epilepsy
familial focal
with variable foci 3
Other Variants in NPRL3
rs886037958 rs886037959 rs886037960 rs886037961 rs886037962 rs1064795838 rs746082270 rs547498080 rs367664536 rs1555444207
Ask Dr. Hemsworth about this variant