NIPA2, NIPA magnesium transporter 2, 81614

N. diseases: 10; N. variants: 2
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: rs3693
rs3693 		1.000 0.040 15 22868175 3 prime UTR variant T/G snv 0.39
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.010 < 0.001 1 2019 2019
dbSNP: rs371775791
rs371775791 		0.925 0.040 15 22866495 missense variant A/G snv 7.2E-05 5.6E-05
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		Nervous System Diseases 0.010 1.000 1 2014 2014
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