Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9375225 1.000 0.040 6 98140878 intron variant G/T snv 0.41 1
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 6
rs9364726 0.882 0.040 6 164236705 intergenic variant A/G snv 6.5E-02 3
rs9362426
SMIM8
1.000 0.040 6 87380156 intron variant A/G;T snv 1
rs9354352 0.882 0.040 6 65986379 intergenic variant T/C snv 0.42 3
rs931913 1.000 0.040 3 36801658 intergenic variant G/A snv 0.31 1
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 7
rs914715
TLE4
1.000 0.040 9 79695983 intron variant T/A snv 0.96 1
rs907162
ASAP2
1.000 0.040 2 9270500 intron variant T/C snv 0.35 1
rs886424
LINC00243
0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 10
rs885553
LINC01121
1.000 0.040 2 45229251 intron variant C/G;T snv 0.54 1
rs884964
ADCY2
1.000 0.040 5 7548741 intron variant T/C snv 0.21 1
rs884301
HLF
1.000 0.040 17 55290103 intron variant C/T snv 0.42 1
rs868094
LOC105374875
1.000 0.040 6 464426 intron variant T/C snv 0.41 1
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 3
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 15
rs8067817 1.000 0.040 17 40007683 downstream gene variant C/G;T snv 1
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 7
rs8031287 1.000 0.040 15 46554008 intron variant C/T snv 0.31 1
rs802568
CNTNAP2
0.925 0.040 7 146262151 intron variant T/G snv 0.17 2
rs7959663
MYO1H
0.925 0.040 12 109446562 intron variant G/A;C snv 2
rs79436609
TRIM42
1.000 0.040 3 140698604 intron variant T/C snv 1.8E-02 2
rs79403677
FAM177A1
0.925 0.040 14 35069925 intron variant T/G snv 0.17 2
rs7939917
TMPRSS5
0.882 0.040 11 113697374 missense variant C/T snv 2.0E-03 9.2E-03 3