Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs995030
KITLG
0.776 0.320 12 88496894 3 prime UTR variant A/G snv 0.67 9
rs886039769
NR5A1
0.807 0.160 9 124500686 missense variant G/A snv 10
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs864622096
PMS2
0.925 0.040 7 5986916 missense variant G/A snv 2
rs8103849
UHRF1 ; ARRDC5
1.000 0.040 19 4909617 missense variant C/G snv 0.38 0.40 1
rs7867029
LOC107987083
0.925 0.040 9 78405502 intergenic variant G/C snv 0.22 3
rs786203623
MLH1
0.925 0.040 3 37017520 missense variant T/A;C snv 2
rs763468927
PMS2
0.925 0.040 7 5977755 missense variant G/A snv 4.0E-06 7.0E-06 2
rs724078 0.925 0.040 6 29521271 intergenic variant G/A snv 0.41 3
rs7174015
USP8
0.925 0.040 15 50424871 intron variant G/A;T snv 3
rs696
NFKBIA
0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45 22
rs61734716
SLC10A6
1.000 0.040 4 86828144 missense variant G/A snv 2.3E-03 1.0E-02 1
rs6166
FSHR
0.708 0.240 2 48962782 missense variant C/T snv 0.57 0.57 17
rs6165
FSHR
0.724 0.160 2 48963902 missense variant C/G;T snv 4.0E-06; 0.55 14
rs6080550
LOC100289473
0.851 0.040 20 1778944 intron variant C/G;T snv 9.6E-02 5
rs587781908
PMS2
0.925 0.040 7 6005973 missense variant A/G snv 1.2E-05 2
rs55763075
MTHFR ; C1orf167
0.827 0.120 1 11790377 3 prime UTR variant C/T snv 2.1E-05 6
rs553509
H2BW1
0.925 0.040 X 104013293 missense variant T/C snv 0.38 3
rs508485
PIWIL4 ; LOC105369438
1.000 0.040 11 94621313 3 prime UTR variant C/T snv 0.49 1
rs4647269
MLH1
0.925 0.040 3 37016100 intron variant C/T snv 0.35 2
rs4474514
KITLG
0.827 0.240 12 88560182 intron variant G/A snv 0.65 6
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs3819392
KIT
1.000 0.040 4 54660528 intron variant G/A snv 0.28 2
rs3791185
PRMT6
1.000 0.040 1 107058247 3 prime UTR variant G/A snv 0.14 1
rs3749897
UBR2
1.000 0.040 6 42564364 missense variant C/G;T snv 0.43 1