Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12118370
ST7L
1 112605645 intron variant A/G snv 0.24 3
rs2999159
MOV10
1 112688136 intron variant A/G snv 0.85 4
rs2072134
OAS3
12 112971371 3 prime UTR variant G/A snv 3.7E-03 3
rs7140110
GAS6 ; GAS6-AS1
13 113841051 non coding transcript exon variant T/C snv 0.28 4
rs9969423
FAM167A-AS1
8 11398066 intron variant A/C snv 0.39 2
rs2484294 10 114032303 intergenic variant G/A snv 0.70 4
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs12108602 4 114719413 upstream gene variant A/G snv 0.18 1
rs4475251 5 115039988 intergenic variant G/A;T snv 3
rs35444 12 115114632 intergenic variant A/G snv 0.38 6
rs35443 12 115115073 intergenic variant G/C snv 0.40 5
rs35441 12 115115310 intergenic variant C/T snv 0.40 5
rs2737216
TRPS1
8 115617852 intron variant A/T snv 0.62 2
rs899366 8 11572976 upstream gene variant G/A;C snv 2
rs2244894 8 11591150 intergenic variant G/C snv 0.45 1
rs13249843 8 11601509 regulatory region variant G/T snv 0.32 2
rs13210143
FRK
6 116068473 intergenic variant G/A snv 0.38 2
rs13280442 8 11610048 intergenic variant C/A;G snv 3
rs13250871 8 11610254 intergenic variant G/A snv 0.28 1
rs509728 11 116662450 downstream gene variant G/C snv 2.7E-02 5
rs3735814
GATA4
8 11749887 intron variant G/A snv 0.54 2
rs36038176
GATA4
8 11752486 intron variant C/G;T snv 2
rs1090107
NEIL2
8 11775019 intron variant A/G;T snv 2
rs72640211
C1orf167-AS1 ; C1orf167
1 11778705 synonymous variant G/A snv 4.4E-02 4.8E-02 1
rs12561919
C1orf167 ; C1orf167-AS1
1.000 0.040 1 11779866 missense variant C/T snv 0.13 0.13 3