Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6746030
SCN1A-AS1 ; SCN9A
0.763 0.320 2 166242648 missense variant A/G snv 0.88 0.88 16
rs2241883
FABP1
0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs11674595
IL1R2
0.763 0.200 2 101994530 intron variant T/C snv 0.22 13
rs10166942
TRPM8
0.925 0.040 2 233916448 upstream gene variant T/C snv 0.40 4
rs11898284
SCN1A-AS1 ; SCN9A
2 166325017 intron variant A/G snv 0.15 1
rs12478318
SCN1A-AS1 ; SCN9A
2 166277030 missense variant T/G snv 3.7E-02 1.3E-02 1
rs4369876
SCN9A ; SCN1A-AS1
2 166272746 missense variant C/A snv 3.3E-02 1.3E-02 1
rs879254102
SCN9A ; SCN1A-AS1
2 166277257 missense variant C/T snv 1
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs6801957
SCN10A
1.000 0.080 3 38725824 intron variant T/C snv 0.67 7
rs138607170
SCN11A
0.882 0.080 3 38925454 missense variant G/A snv 4.0E-06 1.4E-05 4
rs13080116
SCN11A
3 38865732 intron variant T/C snv 0.23 2
rs13093031 1.000 0.120 3 88809891 intergenic variant A/G snv 0.17 2
rs33985936
SCN11A
3 38894643 missense variant C/A;T snv 8.0E-06; 0.22 2
rs376128467
SCN11A
3 38894920 missense variant A/G;T snv 4.0E-06 2
rs11709492
SCN11A
3 38904493 intron variant C/T snv 0.26 1
rs11720013
SCN11A
3 38924745 intron variant G/T snv 1.0E-01 1
rs11720988
SCN11A
3 38865054 intron variant G/A snv 0.26 1
rs12633508 3 88765985 intergenic variant T/C snv 0.23 1
rs4073
CXCL8
0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs7439366
UGT2B7
0.752 0.320 4 69098620 missense variant T/C snv 0.56 0.57 16
rs765502022
UGT2B7
0.827 0.240 4 69112695 missense variant T/C snv 1.6E-05 8
rs749415280
UGT2B7
1.000 0.120 4 69096638 missense variant A/G snv 2