Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs267607165
TUBB3
0.708 0.520 16 89935679 missense variant G/A;C snv 18
rs104893836
UBA6-AS1 ; GNRHR
0.790 0.160 4 67754019 missense variant T/C snv 2.8E-03 2.3E-03 7
rs74315418
PROKR2
0.827 0.160 20 5314116 missense variant C/A;T snv 3.3E-04; 7.1E-04 5
rs1800053
AR
0.851 0.160 X 67711453 missense variant C/A snv 1.1E-03 1.2E-03 4
rs771470596
EDNRA
0.882 0.200 4 147539919 missense variant G/A;C snv 1.6E-05 4
rs1800447
LHB
0.851 0.200 19 49016648 missense variant A/G snv 6.5E-02 7.6E-02 4
rs34349826
LHB
0.851 0.200 19 49016626 missense variant A/G snv 4.9E-02 7.5E-02 4
rs104894897
NR0B1
0.882 0.160 X 30304676 missense variant A/C snv 4
rs78861628
PROKR2
0.851 0.160 20 5302393 missense variant G/A snv 3.9E-03 1.4E-02 4
rs104893844
UBA6-AS1 ; GNRHR
0.882 0.160 4 67754068 missense variant C/T snv 3.6E-05 7.0E-06 4
rs74452732
UBA6-AS1 ; GNRHR
0.851 0.160 4 67753825 missense variant C/A;T snv 4.0E-06 4
rs139767835
AR
0.882 0.160 X 67545280 missense variant C/G snv 3.3E-05 2.5E-04 3
rs148499544
GNRHR ; UBA6-AS1
0.882 0.160 4 67740670 missense variant A/C snv 8.0E-06 5.6E-05 3
rs28935481
NR0B1
0.882 0.160 X 30304673 missense variant T/A;C snv 5.4E-06 3
rs1204919376
SRGN
0.882 0.160 10 69103945 missense variant G/C snv 4.0E-06 3
rs750566506
GNRHR ; UBA6-AS1
0.925 0.160 4 67754013 missense variant T/C snv 2