Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1800866
rs1800866
SIGMAR1
8 0.851 0.080 9 34637693 missense variant T/G snv 0.20 0.18 0.010 1.000 1 2019 2019
dbSNP: rs6334
rs6334
NTRK1
3 1.000 0.080 1 156876441 missense variant G/A;C;T snv 0.22; 4.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs6795970
rs6795970
SCN10A
13 0.807 0.200 3 38725184 missense variant A/G snv 0.65 0.70 0.010 1.000 1 2016 2016
dbSNP: rs943552
rs943552 		2 1 156885826 downstream gene variant C/T snv 9.7E-02 0.010 1.000 1 2018 2018