Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35979828
NFE2
12 54292096 intron variant C/T snv 5.0E-02 9
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 9
rs1613662
GP6 ; LOC107985325
0.851 0.120 19 55025227 missense variant G/A snv 0.85 0.83 8
rs342293
CTB-30L5.1
0.882 0.040 7 106731773 intron variant C/G snv 0.42 7
rs216311
VWF
0.882 0.040 12 6019277 missense variant T/A;C snv 4.0E-06; 0.69 7
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 6
rs6065
CHRNE ; GP1BA
0.851 0.280 17 4933086 missense variant C/T snv 9.8E-02 0.13 6
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 6
rs11553699
TMEM120B ; RHOF
12 121779004 3 prime UTR variant A/G snv 9.4E-02 6
rs7394579
FADS2 ; FADS1
1.000 0.080 11 61813978 intron variant A/G snv 0.22 5
rs11627485
FNTB ; CHURC1-FNTB ; MAX
14 65020976 intron variant T/C snv 0.36 5
rs7896518
JMJD1C
10 63344740 intron variant A/G snv 0.38 5
rs9402686
LOC105378010
6 135106679 upstream gene variant G/A snv 0.20 5
rs114694170
MEF2C ; MEF2C-AS1
1.000 0.040 5 88884379 non coding transcript exon variant T/C snv 3.6E-02 5
rs1569419
PRDM16
1 3080038 intron variant T/C snv 0.73 5
rs78909033
RNPEPL1
2 240571486 intron variant G/A snv 9.2E-02 5
rs13412535
SERPINE2
2 224010157 intron variant G/A snv 0.17 5
rs34651
TNPO1
1.000 0.040 5 72848178 non coding transcript exon variant C/T snv 0.94 5
rs74847330
ARHGAP15
2 143074030 intergenic variant A/G snv 8.8E-02 4
rs1354034
ARHGEF3
3 56815721 intron variant T/C snv 0.49 4
rs56043070
GCSAML
1 247556467 splice donor variant G/A;T snv 5.2E-02; 4.1E-06 4
rs10761741
JMJD1C
1.000 0.040 10 63306426 intron variant G/T snv 0.38 4
rs6141
THPO
0.925 0.080 3 184372478 3 prime UTR variant C/G;T snv 4.0E-06; 0.56 4
rs11734132 4 6889792 intergenic variant G/C snv 0.17 3
rs9378249 0.925 0.160 6 31359924 upstream gene variant T/A;G snv 3