Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2018860
IGF1R
0.925 0.120 15 98715481 intron variant A/C;G;T snv 3
rs234148
LOC105370650
14 97688682 upstream gene variant T/C;G snv 1
rs6234
PCSK1 ; LOC101929710
0.851 0.160 5 96393270 missense variant G/C snv 0.27 0.24 8
rs6235
LOC101929710 ; PCSK1
0.925 0.120 5 96393194 missense variant C/G snv 0.26 0.23 8
rs7713317
LOC101929710
5 96381018 intron variant A/G snv 0.28 3
rs13179048
LOC101929710 ; MIR583HG
5 96207022 intron variant C/A snv 0.23 2
rs4869272
MIR583HG ; LOC101929710
5 96203744 intron variant C/T snv 0.72 3
rs2605627
SMCO4
11 93526349 intron variant A/G snv 0.79 2
rs11782386 8 9344277 intron variant C/T snv 9.7E-02 2
rs143399767 9 93420421 downstream gene variant A/C snv 6.9E-03 1
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 9
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs983309 8 9320222 intron variant T/G snv 0.82 2
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 7
rs2166706 1.000 0.080 11 92958366 intergenic variant T/A;C snv 2
rs7936247 1.000 0.040 11 92956866 intergenic variant G/T snv 0.37 5
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs3847554 11 92935660 upstream gene variant C/T snv 0.56 1
rs8004664
FOXN3
0.925 0.080 14 89568628 intron variant G/A;C snv 3
rs8020333
FOXN3
14 89568505 intron variant C/G;T snv 0.52 2
rs11041816 11 8222251 downstream gene variant A/G snv 0.36 2
rs13427272
CTNNA2
2 80058810 intron variant G/A snv 5.4E-02 1
rs7708285
ZBED3-AS1
1.000 0.080 5 77130042 intron variant G/A snv 0.76 3
rs7821492 8 76910847 intron variant G/A;C;T snv 1