Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11127292
MYT1L
0.925 0.160 2 2026171 intron variant C/T snv 0.11 2
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 29
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1314305899
NOS3
0.807 0.280 7 151003224 missense variant C/T snv 7.9E-06 2.1E-05 6
rs375382379
NR3C1
0.882 0.160 5 143399792 missense variant T/C snv 4.0E-06 5
rs550659379
NR3C1
0.882 0.160 5 143399780 missense variant T/C snv 4.0E-06 7.0E-06 5
rs752834812
NR3C1
0.882 0.160 5 143399885 missense variant T/C snv 8.0E-06 5
rs772651364
NR3C1
0.882 0.160 5 143400050 missense variant C/T snv 4.0E-06 5
rs5522
NR3C2
0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs3771863
TACR1 ; LOC105374811
0.925 0.240 2 75192588 intron variant C/T snv 0.30 2
rs35699176
ZNF77
1.000 0.080 19 2936537 stop gained G/A snv 3.1E-02 3.4E-02 1