Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9991821
SCARB2
1.000 0.040 4 76209132 intron variant G/A snv 0.18 1
rs998382
DNMT3B
1.000 0.040 20 32796330 intron variant A/G snv 0.49 1
rs997944825
ADNP
1.000 0.040 20 50902064 missense variant T/C snv 1
rs997277 1.000 0.040 2 188886137 intergenic variant A/G snv 0.30 1
rs9952724
CTIF
1.000 0.040 18 48726444 intron variant A/C;T snv 1
rs9938550
HSD3B7
1.000 0.040 16 30987821 missense variant A/G;T snv 0.59; 4.0E-06 1
rs9878775
DCUN1D1
1.000 0.040 3 182942165 3 prime UTR variant T/A;C snv 1
rs986952349
MUL1
1.000 0.040 1 20507924 missense variant C/G;T snv 1.4E-05 2.8E-05 1
rs9858038 1.000 0.040 3 183012503 upstream gene variant G/A snv 0.22 1
rs9841498 1.000 0.040 3 183009309 intergenic variant C/T snv 0.43 1
rs983198652
AIMP2 ; SNORA80D
0.925 0.040 7 6015170 missense variant G/A snv 2
rs9822789
MCCC1
1.000 0.040 3 183085086 intron variant G/T snv 0.17 1
rs9808753
IFNGR2
0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs972936
IGF1 ; LINC02456
0.807 0.200 12 102431143 intron variant T/C snv 0.70 12
rs9722
S100B
0.776 0.200 21 46599326 3 prime UTR variant G/A snv 0.16; 2.4E-05 0.21 9
rs9697983
LOC105373328 ; GLUD2
0.925 0.040 X 121049176 missense variant T/G snv 2.7E-02 3.2E-02 2
rs967582
ELAVL4
1.000 0.040 1 50116500 intron variant A/C snv 0.42 1
rs9652490
LINGO1
0.851 0.080 15 77671545 intron variant A/G snv 0.28 4
rs9614
FBXO2
1.000 0.040 1 11650504 missense variant T/G snv 0.22 0.20 1
rs9568188
CAB39L
1.000 0.040 13 49353596 intron variant T/C snv 0.38 1
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs952149887
DNM1L
1.000 0.040 12 32701547 missense variant A/G snv 1
rs9516970
LOC105370324
1.000 0.040 13 97592635 intergenic variant G/A snv 0.56 1
rs947211
LOC105371702
0.925 0.040 1 205783537 non coding transcript exon variant A/G snv 0.64 3
rs9468199 1.000 0.040 6 27713436 downstream gene variant G/A snv 0.26 1