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: rs16476
rs16476
NPY ; LOC107986777
1 7 24290600 intron variant T/G snv 0.44 0.010 1.000 1 2018 2018
dbSNP: rs16979956
rs16979956
BMX ; ACE2
2 X 15525068 intron variant C/T snv 4.0E-04 0.010 1.000 1 2014 2014
dbSNP: rs1783901
rs1783901
SCN3B
1 11 123642798 intron variant C/T snv 0.24 0.010 1.000 1 2018 2018
dbSNP: rs1939012
rs1939012
MMP8
2 1.000 0.040 11 102724404 intron variant T/C snv 0.58 0.010 1.000 1 2018 2018
dbSNP: rs35697037
rs35697037
BMX ; ACE2
2 X 15523993 intron variant G/A snv 0.37 0.010 1.000 1 2014 2014
dbSNP: rs3743077
rs3743077
CHRNA3
3 1.000 0.040 15 78602554 intron variant C/T snv 0.31 0.010 1.000 1 2014 2014
dbSNP: rs7136446
rs7136446
IGF1 ; LINC02456
8 0.882 0.160 12 102444737 intron variant C/T snv 0.66 0.010 1.000 1 2019 2019
dbSNP: rs7178176
rs7178176
CHRNA7
2 15 32151612 intron variant C/T snv 0.18 0.010 1.000 1 2014 2014
dbSNP: rs755204
rs755204
CHRNA4 ; LOC100130587
2 20 63362813 intron variant G/A snv 8.6E-02 0.010 1.000 1 2014 2014
dbSNP: rs7812298
rs7812298
CHRNA6
2 8 42753436 intron variant C/T snv 0.36 0.010 1.000 1 2014 2014
dbSNP: rs7828365
rs7828365
CHRNA6
2 8 42774171 intron variant C/T snv 0.14 0.010 1.000 1 2014 2014
dbSNP: rs972936
rs972936
IGF1 ; LINC02456
12 0.807 0.200 12 102431143 intron variant T/C snv 0.70 0.010 1.000 1 2019 2019
dbSNP: rs144948296
rs144948296
CKMT1B ; STRC
3 0.925 0.120 15 43604750 stop gained G/A;C snv 1.8E-04 0.700 0
dbSNP: rs1799971
rs1799971
OPRM1
95 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 0.020 1.000 2 2013 2018
dbSNP: rs1048101
rs1048101
ADRA1A
5 0.882 0.120 8 26770511 missense variant A/G snv 0.52 0.56 0.010 1.000 1 2018 2018
dbSNP: rs151344517
rs151344517
AFG3L2 ; TUBB6 ; LOC107985154
31 0.742 0.320 18 12337505 missense variant C/T snv 0.700 1.000 1 2010 2010
dbSNP: rs2032582
rs2032582
ABCB1
97 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2012 2012
dbSNP: rs796053124
rs796053124
SCN2A
4 0.882 0.080 2 165354232 missense variant G/T snv 0.700 1.000 1 2010 2010
dbSNP: rs121908216
rs121908216
CACNA1A
7 0.882 0.200 19 13235702 missense variant C/T snv 0.700 0
dbSNP: rs121912683
rs121912683
SLC25A4
9 0.851 0.200 4 185145020 missense variant C/A snv 4.0E-06 7.0E-06 0.700 0
dbSNP: rs28937900
rs28937900
FKRP
37 0.752 0.160 19 46756276 missense variant C/A;T snv 1.0E-03 0.700 0
dbSNP: rs397507478
rs397507478
BRAF
12 0.790 0.440 7 140777014 missense variant C/A snv 0.700 0
dbSNP: rs61755320
rs61755320
SPG7
41 0.716 0.520 16 89546737 missense variant C/T snv 2.9E-03 3.5E-03 0.700 0
dbSNP: rs797045032
rs797045032
CLCN1
11 0.827 0.280 7 143321720 missense variant GG/TC mnv 0.700 0
dbSNP: rs1045642
rs1045642
ABCB1
214 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2012 2012