Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2273267
NRAS ; CSDE1
0.882 0.080 1 114716848 upstream gene variant A/C;T snv 4
rs6744811
SNHG31
1.000 0.040 2 214812584 intron variant A/C;T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs121912443
SOD1
0.732 0.160 21 31663857 missense variant A/G snv 15
rs7652589 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 13
rs121917887
NME1-NME2 ; NME1
0.790 0.120 17 51161744 missense variant A/G snv 6.0E-05 7.0E-05 10
rs110419
LOC105376536 ; LMO1
0.827 0.200 11 8231306 intron variant A/G snv 0.42 8
rs1501899
CASR
0.790 0.240 3 122188481 intron variant A/G snv 0.62 8
rs2168351
ST8SIA2
0.851 0.120 15 92440492 intron variant A/G snv 0.33 6
rs3784730
ST8SIA2
0.851 0.120 15 92443898 intron variant A/G snv 0.44 6
rs11994014 0.827 0.200 8 24944767 intergenic variant A/G snv 0.70 5
rs201216664
NME1-NME2 ; NME2
0.851 0.080 17 51171503 missense variant A/G snv 5
rs74315406
PRNP
0.851 0.160 20 4699870 missense variant A/G snv 5
rs10895322
MMP20
0.851 0.120 11 102599525 intron variant A/G snv 9.4E-02 4
rs6939340
CASC15 ; NBAT1
0.851 0.160 6 22139775 intron variant A/G snv 0.62 4
rs10055201
IL31RA
0.882 0.080 5 55865274 intron variant A/G snv 0.76 3
rs10840002 0.882 0.080 11 8221479 downstream gene variant A/G snv 0.49 3
rs17489363
SNHG31 ; BARD1
0.882 0.080 2 214809617 5 prime UTR variant A/G snv 0.73 0.74 3
rs3768707
BARD1
0.882 0.080 2 214780411 intron variant A/G snv 0.74 3
rs7973450
KRAS
0.882 0.080 12 25208208 3 prime UTR variant A/G snv 0.20 3
rs2367486 1.000 0.040 7 142784320 upstream gene variant A/G snv 0.50 2