Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1465618
THADA
0.882 0.160 2 43326810 intron variant T/C snv 0.80 3
rs6545977 0.882 0.160 2 63074029 regulatory region variant G/A snv 0.50 3
rs10187424
VAMP8
0.925 0.080 2 85567174 intron variant T/A;C snv 2
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 2
rs11902236
GRHL1
0.925 0.080 2 9977740 intron variant C/T snv 0.36 2
rs13385191
LDAH
0.925 0.080 2 20688505 intron variant A/G snv 0.20 2
rs13393577
ERBB4
0.851 0.120 2 212432139 intron variant T/C snv 0.10 2
rs1801278
IRS1
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 2
rs2292884
MLPH
0.925 0.080 2 237534583 missense variant A/G snv 0.28 0.34 2
rs3771570
FARP2
0.925 0.080 2 241443449 3 prime UTR variant C/T snv 0.11 2
rs7584330 0.925 0.080 2 237478585 intergenic variant A/G snv 0.38 2
rs9332964
SRD5A2
0.763 0.240 2 31529325 missense variant C/T snv 4.7E-04 1.6E-04 2
rs10931777
ANKRD44-IT1 ; ANKRD44
1.000 0.080 2 197278867 intron variant C/T snv 0.72 1
rs121434249
SRD5A2
0.851 0.280 2 31529323 missense variant C/G;T snv 4.0E-06 1
rs12618769
MGAT4A
0.882 0.120 2 98623468 3 prime UTR variant C/T snv 0.18 1
rs16824376
PLCL1
1.000 0.080 2 197819618 intron variant C/T snv 0.19 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs1851779
BOLL
1.000 0.080 2 197782384 intron variant C/T snv 0.19 1
rs2293255
BOLL
1.000 0.080 2 197756782 intron variant T/C snv 0.20 1
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 1
rs6707521
PLCL1
1.000 0.080 2 197848507 intron variant G/A snv 0.18 1
rs6727480
ANKRD44-IT1 ; ANKRD44
1.000 0.080 2 197279147 intron variant A/G snv 0.19 1
rs996427
PLCL1
1.000 0.080 2 197820885 intron variant G/A snv 0.20 1
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 22
rs121913396
CTNNB1
0.732 0.200 3 41224607 missense variant A/C;G;T snv 11