Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2235375
IRF6
0.807 0.400 1 209792242 intron variant G/A;C;T snv 3.2E-05; 0.41; 4.3E-04 7
rs4752028
SHTN1
0.807 0.200 10 117075480 intron variant C/T snv 0.73 6
rs10130587
BMP4
0.851 0.200 14 53952392 intron variant G/C snv 0.45 5
rs2326398
CRISPLD2
0.827 0.200 16 84869111 intron variant A/G snv 0.37 5
rs493760
DROSHA
0.851 0.200 5 31436933 intron variant C/T snv 0.74 5
rs560426
ABCA4
0.851 0.200 1 94087882 intron variant C/T snv 0.53 5
rs1139
ZNF385B
0.851 0.200 2 179745354 intron variant C/T snv 0.22 4
rs197204
MCUB
0.851 0.200 4 109576918 intron variant C/G snv 0.52 4
rs6757845
ZNF385B
0.851 0.200 2 179449268 intron variant T/C snv 0.66 4
rs2076056
JARID2
0.882 0.200 6 15487551 intron variant C/A;G;T snv 0.24 3
rs2237138
JARID2
0.882 0.200 6 15463164 intron variant T/C snv 0.22 3
rs227493 0.882 0.200 6 165071698 intron variant A/T snv 1.7E-02 3
rs3905385
ROR2
0.882 0.200 9 91906451 intron variant T/C snv 0.23 3
rs642961 0.732 0.440 1 209815925 intergenic variant A/G snv 0.84 14
rs13041247
LOC102724968
0.851 0.200 20 40640434 regulatory region variant T/C snv 0.36 5
rs398124401
SRD5A3
0.695 0.480 4 55346393 stop gained G/A snv 1.2E-04 2.8E-05 26
rs587784105
NSD1
0.732 0.440 5 177235863 stop gained G/A snv 19
rs765379963
TMCO1
0.701 0.520 1 165743172 stop gained G/A snv 1.2E-05 2.1E-05 19
rs771409809
WFS1
0.732 0.480 4 6301794 stop gained C/T snv 6.0E-05 7.0E-06 19
rs369867819
LOC107984360 ; LRRC32
0.851 0.320 11 76659963 stop gained G/A;T snv 4.0E-06 5
rs1554985320
PAX6
0.925 0.240 11 31801619 stop gained C/T snv 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
rs79184941
FGFR2
0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 41
rs752746786
GNB1
0.742 0.560 1 1806503 missense variant A/C;G;T snv 4.0E-06 30