Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333017606
GPC2 ; STAG3
1.000 0.080 7 100175622 missense variant C/G;T snv 4.0E-06; 8.0E-06 1
rs144940475
TMTC4
1.000 0.080 13 100612442 missense variant T/C snv 1.4E-04; 8.1E-06 4.1E-04 1
rs17094222 0.925 0.080 10 100635683 intergenic variant T/C snv 0.17 1
rs1235690743
LZTS2
1.000 0.080 10 101003969 missense variant G/C snv 4.0E-06 7.0E-06 1
rs763258401
LOC105373512 ; MIR5696 ; RNF149
1.000 0.080 2 101308570 stop gained C/A;T snv 6.0E-06 1
rs140657361
UTP20
1.000 0.080 12 101352104 missense variant A/T snv 3.4E-04 1.5E-03 1
rs6214
LINC02456 ; HELLPAR ; IGF1
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 1
rs3774937
NFKB1
0.776 0.280 4 102513096 intron variant T/C snv 0.26 5
rs1386751319
SLC9A2
1.000 0.080 2 102665242 missense variant C/G snv 2.0E-05 1
rs4919687
CYP17A1
0.742 0.160 10 102835491 non coding transcript exon variant G/A snv 0.25 9
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs4684677
GHRLOS ; GHRL
0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 1
rs281439
ICAM5
0.925 0.080 19 10289434 upstream gene variant G/C;T snv 1
rs750014974
COL11A1
1.000 0.080 1 102913687 missense variant G/T snv 1.2E-05 1
rs280519
TYK2
0.752 0.320 19 10362257 splice region variant A/C;G snv 0.50 2
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs7907606 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 5
rs1092913
ROPN1L
0.925 0.080 5 10467590 intron variant G/A snv 0.19 1
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 2
rs150456818
MYHAS ; MYH1
1.000 0.080 17 10496414 missense variant C/T snv 8.4E-05 2.9E-04 1
rs139860229
MYHAS ; MYH1
1.000 0.080 17 10497766 missense variant C/T snv 5.6E-05 8.4E-05 1
rs752643679
MYH1 ; MYHAS
1.000 0.080 17 10499041 missense variant G/A snv 3.6E-05 2.1E-05 1
rs616488
PEX14
0.925 0.080 1 10506158 intron variant A/G snv 0.27 2
rs9790517
TET2
0.925 0.080 4 105163621 intron variant C/T snv 0.20 2
rs1298422772
FKTN
1.000 0.080 9 105607844 missense variant G/A snv 7.0E-06 1