Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs762285755
CUBN
0.925 0.160 10 17114074 missense variant T/C snv 7.6E-05 2.8E-05 2
rs759853
AKR1B1
0.827 0.320 7 134459206 non coding transcript exon variant G/A snv 0.33 6
rs7588550
ERBB4
0.851 0.160 2 212304043 intron variant G/A snv 0.96 4
rs758130759
HNF1B
0.925 0.120 17 37699149 missense variant C/T snv 1.6E-05 1.4E-05 3
rs7577
CNDP2
1.000 0.120 18 74521112 3 prime UTR variant T/A;C;G snv 0.21 1
rs75444904
HPR ; TXNL4B
0.851 0.160 16 72061751 intron variant A/C snv 2.4E-02 4
rs751141
EPHX2
0.732 0.400 8 27516348 missense variant G/A snv 0.12 0.10 16
rs745452033
SLC12A3
0.925 0.160 16 56865465 missense variant G/C snv 4.0E-06 7.0E-06 2
rs743507
NOS3
0.882 0.200 7 151010400 intron variant C/T snv 0.77 4
rs741301
ELMO1
0.925 0.160 7 36878390 intron variant C/T snv 0.59 3
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs735853
MYH9
1.000 0.120 22 36283169 intron variant C/G snv 0.34 1
rs73206603
LOC107984625
0.882 0.160 13 59495931 regulatory region variant G/C snv 4.2E-02 3
rs7222331
KRTAP3-3
0.925 0.120 17 40995605 upstream gene variant C/T snv 0.24 3
rs7212142
RPTOR
0.827 0.200 17 80650141 intron variant G/A snv 0.50 5
rs7211818
RPTOR
0.827 0.200 17 80715103 intron variant A/G snv 0.23 5
rs713041
GPX4
0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
rs710218
SLC2A1-AS1
0.882 0.280 1 42961547 intron variant T/A snv 0.38 5
rs6997279
SLC30A8
0.882 0.160 8 116961613 intron variant G/T snv 0.20 3
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs6930576
SASH1
1.000 0.120 6 148383818 intron variant G/A snv 0.36 1
rs688
LDLR
0.742 0.400 19 11116926 synonymous variant C/T snv 0.39 0.34 16
rs6704078 0.925 0.200 1 216437370 intergenic variant C/T snv 0.94 2
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157