Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs414580
MSR1
0.882 0.120 8 16177793 intron variant T/A;C snv 3
rs4237770
LMO1
0.882 0.120 11 8254288 intron variant T/C snv 0.37 3
rs442264
LMO1
0.882 0.120 11 8242602 intron variant G/A snv 0.44 3
rs525549
KMT2A
0.882 0.120 11 118487353 intron variant T/A snv 0.33 3
rs6461639
RAPGEF5
0.882 0.120 7 22147337 intron variant T/A;C snv 3
rs7039798
FPGS
0.882 0.120 9 127794947 intron variant G/A;C snv 3
rs7286979
EP300
0.882 0.120 22 41102623 intron variant G/A snv 0.26 3
rs7809758
DDC ; FIGNL1
0.882 0.120 7 50505635 intron variant A/G snv 0.36 3
rs880028
FIGNL1 ; DDC
0.882 0.120 7 50502438 intron variant A/G snv 0.21 3
rs17007695 0.851 0.120 4 141788570 intergenic variant T/C snv 7.7E-02 4
rs4748793 0.851 0.120 10 22194082 intergenic variant A/G snv 0.18 4
rs755001634
FOLH1
0.763 0.280 11 49154384 stop gained G/A snv 1.2E-05 13
rs35201683
HFE
0.732 0.360 6 26094205 stop gained C/A;T snv 1.4E-03 12
rs780246573
HFE ; LOC108783645
0.732 0.360 6 26092860 stop gained C/G;T snv 4.0E-06; 8.0E-06 12
rs80338880
TFR2
0.732 0.360 7 100633100 stop gained G/C snv 7.0E-06 12
rs797045145
HFE ; LOC108783645
0.807 0.240 6 26091479 stop gained G/A snv 6
rs368005287
CYP3A4
0.882 0.120 7 99762071 stop gained C/T snv 1.2E-05 7.0E-06 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174