Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1187120 0.925 0.040 6 34182850 intergenic variant T/C snv 0.99 3
rs10407447
PLD3
1.000 0.040 19 40363275 intron variant A/G snv 0.20 1
rs1130399
HLA-DQB1
1.000 0.040 6 32661978 missense variant G/A;T snv 0.20 1
rs11556510
TOMM40
1.000 0.040 19 44891562 missense variant T/G snv 9.8E-03 1.2E-02 1
rs11667768
PLD3 ; C19orf47
1.000 0.040 19 40348525 5 prime UTR variant C/T snv 6.3E-02 0.11 1
rs1334496 1.000 0.040 X 137178554 intergenic variant C/A;T snv 1
rs227959 1.000 0.040 17 3406923 upstream gene variant C/T snv 1
rs2534672
MICB
1.000 0.040 6 31497781 intron variant G/C snv 0.32 1
rs4829605 1.000 0.040 X 137182822 intergenic variant C/A;G snv 1
rs640476 1.000 0.040 5 161277998 intergenic variant T/G snv 0.42 1
rs774321998
C1orf167 ; MTHFR
1.000 0.040 1 11790683 missense variant T/C snv 4.0E-06 7.0E-06 1
rs8052688
UBE2I
1.000 0.040 16 1322182 intron variant G/A;C snv 1
rs8063
UBE2I
1.000 0.040 16 1324817 3 prime UTR variant A/C;G snv 4.0E-06; 4.0E-06; 0.71 1
rs9527025
KL
1.000 0.040 13 33054056 missense variant G/C;T snv 0.14 1
rs669
A2M ; KLRG1
0.851 0.080 12 9079672 missense variant T/C snv 0.31 0.33 7
rs10119
TOMM40
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28 5
rs610932
MS4A6A
0.851 0.080 11 60171834 downstream gene variant T/G snv 0.57 5
rs11767557
EPHA1-AS1
0.882 0.080 7 143412046 intron variant T/C snv 0.18 4
rs11887120
DNMT3A
0.882 0.080 2 25262866 intron variant C/T snv 0.45 4
rs12344615
UBQLN1
0.851 0.080 9 83666280 intron variant A/C;G snv 4
rs16947151
ABI3
0.882 0.080 17 49213276 intron variant A/G snv 0.12 4
rs2070045
SORL1
0.851 0.080 11 121577381 synonymous variant T/G snv 0.32 0.23 4
rs541458 0.851 0.080 11 86077309 regulatory region variant C/T snv 0.71 4
rs59007384
TOMM40
0.851 0.080 19 44893408 intron variant G/A;T snv 4
rs5978930
ANOS1
0.882 0.080 X 8642266 intron variant T/C;G snv 4