Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 35
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs9472135
LOC107986598
0.925 0.120 6 43842065 intron variant T/A;C;G snv 9
rs7740107
L3MBTL3
1.000 0.080 6 130053316 intron variant T/A;G snv 6
rs1256061
ESR2
14 64236875 intron variant G/A;T snv 5
rs218264 4 54542708 intergenic variant A/G;T snv 5
rs62160676
MIR4435-2HG
2 111410354 intron variant T/C;G snv 5
rs2337106
SMAD7
18 48934533 intron variant C/A;G snv 4
rs60695258
AFF1
4 87101557 intron variant C/A;T snv 4
rs7447593
SLC34A1
5 177397136 non coding transcript exon variant C/G;T snv 4
rs9330813
WNT7B
1.000 0.040 22 45968281 intron variant G/A;C snv 4
rs115986297
GMDS
6 2050557 intron variant A/C;G snv 3
rs149804345 3 56710234 intergenic variant AACAAA/-;AACAAAAACAAA;AACAAAAACAAAAACAAA delins 3
rs1997595 21 15205839 intron variant A/C;G snv 3