Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34976449
RERE
1 8438266 3 prime UTR variant -/G delins 0.66 1
rs59073566
LOC101928994
10 69215315 downstream gene variant -/T;TT delins 1
rs71973827
LOC105369568
11 128612542 downstream gene variant A/- delins 0.14 1
rs34338164
PLEK
2 68388414 missense variant A/C snv 8.0E-03 7.8E-03 4
rs17041439
SPIC
12 101479462 intron variant A/C snv 7.0E-02 2
rs9379851 6 26354552 regulatory region variant A/C snv 7.6E-02 2
rs990171 1.000 0.080 2 102470310 upstream gene variant A/C snv 0.78 2
rs17370519
MBNL1
3 152390773 intron variant A/C snv 0.12 1
rs2134794
ERCC3
2 127273303 intron variant A/C snv 0.20 1
rs2224234 14 102915701 downstream gene variant A/C snv 0.33 1
rs4522104 10 98127275 intergenic variant A/C snv 0.15 1
rs4826685 X 3737519 intergenic variant A/C snv 0.34 1
rs6433895
LINC01934
2 181147287 intron variant A/C snv 0.31 1
rs6725295
KLHL23 ; PHOSPHO2-KLHL23
2 169743180 intron variant A/C snv 0.79 1
rs6911302
RIPOR2
6 24819824 intron variant A/C snv 0.46 1
rs13092376
PAK2
3 196789417 intron variant A/C;G snv 0.33 3
rs7192652
NLRC5
16 57041268 intron variant A/C;G snv 2
rs11024625
GTF2H1 ; LOC105376577
11 18350013 intron variant A/C;G snv 1
rs16971368 15 79811833 regulatory region variant A/C;G snv 1
rs380691
MSH3 ; DHFR
5 80656215 intron variant A/C;G snv 1
rs4355658
CLDN4
7 73811362 intron variant A/C;G snv 0.65 1
rs6445528
SMIM4
3 52538431 intron variant A/C;G snv 1
rs139515
RANGAP1
22 41260129 intron variant A/C;G;T snv 1
rs2649662 11 57585089 regulatory region variant A/C;T snv 1
rs4414876
CGGBP1 ; ZNF654
3 88133918 intron variant A/C;T snv 1