Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 7
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 6
rs13125101 4 80253438 TF binding site variant G/A snv 0.24 6
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs2643826 3 27521497 upstream gene variant C/T snv 0.56 6
rs415895
SWAP70
11 9748015 missense variant C/G snv 0.62 0.61 6
rs72681869
SOS2
14 50188639 missense variant G/A;C snv 4.0E-06; 4.1E-03 6
rs7890572
IL1RAPL1
X 29622701 intron variant A/G snv 9.3E-02 6
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs12258967
CACNB2
10 18439030 intron variant C/G;T snv 5
rs12978472
INSR
19 7257979 intron variant C/G;T snv 5
rs167479
RGL3
19 11416089 missense variant T/A;C;G snv 5
rs1894400
FES
15 90885725 intron variant C/T snv 0.28 5
rs3790604
WNT2B
1 112504257 intron variant C/A snv 7.8E-02 5
rs62434109
PLEKHG1
6 150654176 intron variant T/G snv 8.4E-02 5
rs7125196
LOC105369329
11 61505093 intron variant T/C snv 0.16 5
rs7246865
MYO9B
19 17108295 intron variant G/A snv 0.36 5
rs1063857
VWF
12 6044348 synonymous variant A/G snv 0.31 0.40 4
rs10769254
MYBPC3
11 47340914 intron variant G/C snv 0.27 4
rs139491786
SLC9A3R2
16 2036420 missense variant C/T snv 3.4E-03 3.5E-03 4
rs17725246
NPC1L1
7 44542387 upstream gene variant T/A;C snv 4
rs34042070
TXNL4B ; HPR
16 72067626 intron variant C/G snv 0.17 4
rs3735533
HOTTIP
7 27206274 non coding transcript exon variant T/C snv 0.93 4