Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16847024
GC
0.882 0.120 4 71784962 intron variant C/T snv 3.2E-02 4
rs3733359
GC
0.925 0.120 4 71784057 splice region variant G/A snv 0.12; 4.2E-06 0.13 3
rs2254514
IL15
4 141719385 5 prime UTR variant T/A;C snv 1
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs34309
PIK3R1
5 68268555 intron variant G/A snv 0.29 2
rs10068521
PRLR
5 35230278 5 prime UTR variant G/A;C snv 1
rs13154178
SELENOP
5 42827999 intron variant G/A snv 0.31 1
rs9292578
PRLR
5 35229973 intron variant C/A;G snv 1
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs3025039
VEGFA
0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs2146323
VEGFA
0.752 0.480 6 43777358 non coding transcript exon variant C/A snv 0.31 13
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs7754840
CDKAL1
0.807 0.200 6 20661019 intron variant G/A;C;T snv 9
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 7
rs9379084
RREB1
0.882 0.160 6 7231610 missense variant G/A snv 0.11 8.9E-02 6
rs833069
VEGFA
0.851 0.200 6 43774842 non coding transcript exon variant T/C;G snv 5
rs9465871
CDKAL1
0.882 0.120 6 20717024 intron variant T/C snv 0.30 4
rs2021966
ENPP1
1.000 0.080 6 131829299 intron variant A/G snv 0.42 2
rs6456368
CDKAL1
1.000 0.080 6 20659575 intron variant T/C snv 0.40 2