Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11591741
CHUK
1.000 0.080 10 100216744 intron variant G/C snv 0.30 1
rs746722465
FANCD2
1.000 0.080 3 10042563 missense variant G/A snv 8.0E-06 1.4E-05 1
rs35927125
KLF11
0.925 0.080 2 10046292 missense variant A/G;T snv 9.3E-02 3
rs34336420
KLF11
0.882 0.080 2 10047996 missense variant C/G;T snv 4.0E-06; 3.3E-03 4
rs121912645
KLF11
0.882 0.080 2 10048376 missense variant G/T snv 1.3E-04 8.4E-05 4
rs2073162
TNMD
1.000 0.080 X 100594020 synonymous variant G/A snv 0.40 0.39 2
rs2073163
TNMD
0.925 0.120 X 100594054 intron variant T/C snv 0.41 0.39 2
rs1155974
TNMD
0.925 0.120 X 100598284 intron variant C/T snv 0.34 2
rs507392
EPO
0.925 0.160 7 100722313 intron variant G/A;C snv 2
rs551238
EPO
0.925 0.160 7 100723905 downstream gene variant G/T snv 0.62 5
rs7158663
MEG3
0.827 0.240 14 100853087 non coding transcript exon variant A/G snv 0.42 9
rs72928364
ABI3BP
1.000 0.080 3 100894935 intron variant C/T snv 0.39 2
rs6092
SERPINE1
0.807 0.200 7 101128436 missense variant G/A snv 9.5E-02 8.0E-02 6
rs10895068
PGR ; PGR-AS1
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs948516
PGR-AS1
1.000 0.080 11 101139202 intron variant A/G snv 0.23 1
rs1384565 1.000 0.080 15 101264707 intergenic variant T/C snv 3.8E-02 1
rs78900934 1.000 0.080 1 101272565 upstream gene variant C/A snv 0.32 2
rs6598475
PCSK6
1.000 0.080 15 101446425 intron variant G/T snv 0.63 1
rs6543087
MAP4K4
1.000 0.080 2 101699471 intron variant A/G;T snv 2
rs11674694
MAP4K4
1.000 0.080 2 101708862 intron variant C/T snv 0.27 1
rs78789647
DNMT1
1.000 0.080 19 10182225 intron variant C/A;T snv 3.6E-02 1
rs2236935
MAP4K4
1.000 0.080 2 101827580 intron variant C/T snv 0.83 1
rs117168171 1.000 0.080 15 101854599 downstream gene variant C/G;T snv 2
rs994411260
DNMT1
0.925 0.160 19 10194877 missense variant G/C snv 2
rs2607653
FGF14
1.000 0.080 13 102066314 intron variant A/G snv 5.9E-02 2