Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10073892
SLCO6A1
5 102391066 non coding transcript exon variant T/C snv 0.24 0.21 1
rs1049564
PNP
0.882 0.160 14 20472447 missense variant G/A snv 0.19 0.21 6
rs10512015
ANXA1
9 73166330 intron variant T/C snv 9.9E-02 1
rs10524523
TOMM40
0.807 0.200 19 44899792 intron variant TTTTTTTTTTTTTTTTTTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT delins 7
rs1057518919
PSEN1
0.851 0.120 14 73171023 missense variant T/G snv 5
rs11030108
BDNF ; BDNF-AS
1.000 0.040 11 27673917 intron variant A/G snv 0.72 3
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs112422930
MUTYH
0.882 0.160 1 45332409 missense variant A/C snv 7.0E-06 4
rs1126680
BCHE
0.851 0.160 3 165837337 synonymous variant C/T snv 5.6E-02 5.6E-02 5
rs1143684
NQO2
0.882 0.160 6 3010156 missense variant C/T snv 0.79 0.84 4
rs1157659 1.000 0.040 11 27736075 intron variant A/G snv 0.37 2
rs115881343
TOMM40
1.000 0.040 19 44899959 intron variant C/G;T snv 2.9E-02 2
rs1187120 0.925 0.040 6 34182850 intergenic variant T/C snv 0.99 3
rs11887120
DNMT3A
0.882 0.080 2 25262866 intron variant C/T snv 0.45 4
rs1206642175
ESR1
0.925 0.080 6 151808263 synonymous variant G/A snv 7.0E-06 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121912433
SOD1
0.827 0.120 21 31663841 missense variant G/A snv 4.0E-06 7
rs121912456
SOD1 ; LOC102724449
0.851 0.120 21 31659806 missense variant G/C snv 6
rs12273363
BDNF
0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11
rs13333659
CBFA2T3
1.000 0.040 16 88972472 intron variant G/T snv 0.13 2
rs1372439127
GRN
0.925 0.080 17 44352420 missense variant A/G snv 4.0E-06 3
rs1396086494
APP
0.851 0.080 21 26051069 missense variant G/A snv 4.0E-06 6
rs139650807
LRP10
0.925 0.080 14 22875867 missense variant T/A;C snv 6.0E-05 3
rs1427575965
C2orf42 ; TIA1
0.925 0.120 2 70212796 missense variant G/A snv 8.0E-06 3