Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs322
LPL
8 19961706 intron variant A/C snv 0.31 1
rs7046999
LOC105376214
9 108103777 regulatory region variant A/C snv 2.8E-02 1
rs7476
CREB3L1
11 46321284 3 prime UTR variant A/C snv 0.46 1
rs9747201
SLC16A3
17 82219976 downstream gene variant A/C snv 0.76 1
rs10757269
CDKN2B-AS1
1.000 0.040 9 22072265 intron variant A/C;G snv 4
rs12520838
COMMD10
5 116161170 intron variant A/C;G snv 0.10 1
rs6570628
UTRN
6 144428223 intron variant A/C;G;T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs2853669
TERT
0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs2735940
TERT
0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 25
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs5742905
CBS
0.701 0.360 21 43063074 missense variant A/G snv 22
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 13
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
rs3825807
ADAMTS7
0.807 0.120 15 78796769 missense variant A/G snv 0.34 0.33 10
rs1194897557
MTHFR
0.827 0.240 1 11796276 missense variant A/G snv 8.0E-06 7
rs11466653
TLR10
1.000 0.080 4 38774614 missense variant A/G snv 6.4E-02 4.1E-02 3
rs9557207
UBAC2
13 99384164 intron variant A/G snv 0.17 2
rs10467515 13 52927172 regulatory region variant A/G snv 1.2E-02 1
rs11190074
CNNM1
10 99361961 intron variant A/G snv 8.7E-02 1
rs1539189
PDYN-AS1
20 1966633 intron variant A/G snv 2.0E-02 1
rs16855732
TNIK
3 171063141 3 prime UTR variant A/G snv 2.4E-02 1