Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs5361
SELE ; C1orf112
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs11556218
IL16
0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs6136
SELP
0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 17
rs11077
POLR1C ; XPO5
0.732 0.320 6 43523209 3 prime UTR variant T/G snv 0.47 14
rs2243115
IL12A-AS1 ; IL12A
0.776 0.320 3 159988493 intron variant T/G snv 0.10 12
rs602633 0.851 0.080 1 109278889 downstream gene variant T/G snv 0.63 10
rs146292819
ABCA1
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04 9
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs1051338
LIPA
0.807 0.120 10 89247603 missense variant T/G snv 0.32 0.26 7
rs9289231
KALRN
0.827 0.120 3 124055231 intergenic variant T/G snv 0.15 5
rs1870634 0.851 0.080 10 43985363 downstream gene variant T/G snv 0.59 4
rs640198
MMP13
0.851 0.040 11 102954362 intron variant T/G snv 0.68 4
rs35511654
TMIGD3 ; ADORA3
0.882 0.040 1 111500165 missense variant T/G snv 9.4E-02 9.8E-02 3
rs3744700
CXCL16
0.882 0.080 17 4734715 intron variant T/G snv 0.66 3
rs3805489
PRKAA1
0.882 0.040 5 40793242 intron variant T/G snv 0.22 3
rs5705
REN
0.882 0.040 1 204162058 synonymous variant T/G snv 0.14 0.18 3
rs10818576
DAB2IP
1.000 0.040 9 121650669 intron variant T/G snv 0.21 2
rs2047009 0.925 0.080 10 44044465 regulatory region variant T/G snv 0.39 2
rs659418
SERPINH1
1.000 0.040 11 75573289 downstream gene variant T/G snv 0.19 2
rs10913733
SOAT1
1.000 0.040 1 179347934 intron variant T/G snv 8.7E-02 1