rs1164174661, CACNA1A

N. diseases: 3
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.
Benign paroxysmal vertigo of childhood
1 0.925 0.120 19 13283358 missense variant T/C snv 0.010 1.000 1 2008 2008
Hemiplegic migraine
CUI: C0270862
Disease: Hemiplegic migraine
14 0.925 0.120 19 13283358 missense variant T/C snv 0.010 1.000 1 2008 2008
Torticollis
CUI: C0040485
Disease: Torticollis
10 0.925 0.120 19 13283358 missense variant T/C snv 0.010 1.000 1 2008 2008