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: rs1799971
rs1799971
OPRM1
95 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 0.010 1.000 1 2019 2019
dbSNP: rs324420
rs324420
FAAH
48 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 0.010 1.000 1 2019 2019
dbSNP: rs4680
rs4680
COMT ; MIR4761
249 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 0.010 1.000 1 2019 2019
dbSNP: rs745525088
rs745525088
ANK1
1 8 41714203 missense variant C/G;T snv 4.8E-06; 2.4E-05 0.010 1.000 1 2011 2011
dbSNP: rs748409227
rs748409227
ANK1
2 8 41708865 synonymous variant C/T snv 1.6E-05 7.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs8065080
rs8065080
TRPV1
11 0.827 0.200 17 3577153 missense variant T/C snv 0.37 0.32 0.010 1.000 1 2011 2011
dbSNP: rs920829
rs920829
TRPA1 ; MSC-AS1
3 0.925 0.160 8 72065468 missense variant C/T snv 0.14 0.16 0.010 1.000 1 2011 2011