Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28938172
PARK7
0.790 0.080 1 7984981 missense variant T/C snv 7
rs63751163
PSEN1
0.807 0.120 14 73192844 missense variant T/C snv 7
rs1057520018
STK11
0.807 0.080 19 1223124 missense variant T/C snv 6
rs11037575
HSD17B12
0.882 0.080 11 43706780 intron variant T/C snv 0.36 4
rs11103603 0.851 0.080 9 134449754 TF binding site variant T/C snv 0.46 4
rs1468034466
TFRC
0.851 0.120 3 196074028 synonymous variant T/C snv 4
rs201668878
UBE4A
0.882 0.080 11 118373576 missense variant T/C snv 1.7E-04 1.0E-04 4
rs3768716
BARD1
0.851 0.080 2 214771070 intron variant T/C snv 0.16 4
rs110420
LMO1 ; LOC105376536
0.882 0.080 11 8231502 intron variant T/C snv 0.42 3
rs1415224147
MAPKAP1
0.882 0.080 9 125585715 missense variant T/C snv 3
rs1442511697
ADRA2B
0.882 0.080 2 96115494 missense variant T/C snv 7.0E-06 3
rs773249771
ADRA1A
0.882 0.080 8 26864314 missense variant T/C snv 1.2E-05 3
rs867182279
EGFR
0.882 0.080 7 55205510 missense variant T/C snv 3
rs11769443
TRGV9
1.000 0.040 7 38317474 missense variant T/C snv 0.39 0.42 1
rs11980080
TRGV9
1.000 0.040 7 38317593 5 prime UTR variant T/C snv 5.7E-02 1
rs17113407 1.000 0.040 14 22020341 intergenic variant T/C snv 6.7E-02 1
rs17161949 1.000 0.040 1 143550435 intron variant T/C snv 6.4E-02 1
rs17171331 1.000 0.040 7 38323356 upstream gene variant T/C snv 1
rs17496969 1.000 0.040 7 38324688 upstream gene variant T/C snv 5.5E-02 1
rs2240832 1.000 0.040 7 38289412 downstream gene variant T/C snv 0.27 1
rs2240845
TRGV9
1.000 0.040 7 38318811 5 prime UTR variant T/C snv 0.38 1
rs2331599 1.000 0.040 14 22268778 intron variant T/C snv 0.39 1
rs2735179 1.000 0.040 7 38325004 upstream gene variant T/C snv 0.29 1
rs2736964 1.000 0.040 7 38305168 upstream gene variant T/C snv 0.51 1
rs3790171
LOC100130264 ; SLC24A3
1.000 0.040 20 19277749 intron variant T/C snv 0.16 1