NIPA2, NIPA magnesium transporter 2, 81614

N. diseases: 10; N. variants: 2
Disease: Childhood Absence Epilepsy ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs371775791
rs371775791 		0.925 0.040 15 22866495 missense variant A/G snv 7.2E-05 5.6E-05
CUI: C4281785
Disease: Childhood Absence Epilepsy
Childhood Absence Epilepsy 		Nervous System Diseases 0.010 1.000 1 2014 2014