rs1553245943, ATP1A2

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Overgrowth
CUI: C1849265
Disease: Overgrowth
93 1.000 0.080 1 160137001 missense variant G/A snv 0.700 1.000 12 1992 2017
Hemiplegic migraine, familial type 1
CUI: C1832884
Disease: Hemiplegic migraine, familial type 1
37 1.000 0.080 1 160137001 missense variant G/A snv 0.700 1.000 4 2008 2017