Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 23
rs6687758 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 10
rs3849942
C9orf72 ; LOC107987057
0.776 0.200 9 27543283 non coding transcript exon variant T/A;C snv 6
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 6
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 5
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 5
rs7224296
LRRC37A2 ; NSF
0.882 0.160 17 46722680 intron variant G/A snv 0.59 3
rs7571971
EIF2AK3
1.000 0.120 2 88595833 non coding transcript exon variant T/C snv 0.70 0.77 2
rs242557
MAPT
0.752 0.200 17 45942346 intron variant G/A snv 0.36 2
rs1768208
MOBP
0.851 0.200 3 39481512 intron variant T/C snv 0.76 2
rs1411478
STX6
0.925 0.120 1 180993146 intron variant A/G snv 0.56 2
rs114573015 1.000 0.120 1 85137368 downstream gene variant A/G snv 1.1E-02 1
rs12125383 1.000 0.120 1 221995092 regulatory region variant G/A snv 0.14 1
rs2142991 1.000 0.120 10 42845657 intergenic variant C/G;T snv 1
rs6852535 1.000 0.120 4 122557561 intergenic variant G/A snv 0.24 1
rs2045091
ASAP1
1.000 0.120 8 130063613 intron variant C/T snv 0.15 1
rs886039227
DCTN1
0.925 0.200 2 74378123 missense variant A/C snv 1
rs6547705
LOC105374846 ; CD8B
1.000 0.120 2 86817193 intron variant G/A snv 0.83 1
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 1
rs63751391
MAPT
0.882 0.120 17 46010395 missense variant G/T snv 1
rs10675541
MOBP
1.000 0.120 3 39468795 intron variant -/CA delins 1
rs621042
PIK3C2G
1.000 0.120 12 18636073 intron variant C/A snv 0.36 1
rs137853058
PRKN
0.882 0.120 6 161973401 missense variant C/T snv 1.2E-05 1
rs35740963
RUNX2
1.000 0.120 6 45531876 intron variant -/T delins 1
rs11568563
SLCO1A2
0.925 0.240 12 21304500 missense variant T/G snv 4.5E-02 4.4E-02 1