rs121908211, CACNA1A

N. diseases: 5
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.
Hemiplegic migraine, familial type 1
37 0.882 0.080 19 13371744 missense variant C/T snv 0.810 1.000 11 1996 2017
Familial Hemiplegic Migraine
CUI: C0338484
Disease: Familial Hemiplegic Migraine
17 0.882 0.080 19 13371744 missense variant C/T snv 0.030 1.000 3 2005 2015
Migraine with Aura
CUI: C0154723
Disease: Migraine with Aura
56 0.882 0.080 19 13371744 missense variant C/T snv 0.010 1.000 1 2017 2017
Muscle Weakness
CUI: C0151786
Disease: Muscle Weakness
87 0.882 0.080 19 13371744 missense variant C/T snv 0.010 1 2005 2005
Paresis
CUI: C0030552
Disease: Paresis
49 0.882 0.080 19 13371744 missense variant C/T snv 0.010 1 2005 2005