Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2631367
MIR3936HG ; SLC22A5
0.925 0.120 5 132369766 5 prime UTR variant C/G snv 0.59 4
rs10459953
NOS2
0.925 0.080 17 27800492 5 prime UTR variant C/A;G;T snv 3
rs1059060
PMS2
0.925 0.040 7 5977709 missense variant T/A;C snv 3
rs12348
TUSC1
0.925 0.040 9 25677217 3 prime UTR variant T/C snv 0.44 3
rs12870438
EPSTI1
0.925 0.040 13 42906069 intron variant G/A snv 0.27 3
rs553509
H2BW1
0.925 0.040 X 104013293 missense variant T/C snv 0.38 3
rs7174015
USP8
0.925 0.040 15 50424871 intron variant G/A;T snv 3
rs724078 0.925 0.040 6 29521271 intergenic variant G/A snv 0.41 3
rs7867029
LOC107987083
0.925 0.040 9 78405502 intergenic variant G/C snv 0.22 3
rs10129954
DPF3
1.000 0.040 14 72683993 intron variant C/T snv 0.49 2
rs10966811 1.000 0.040 9 25233486 intergenic variant G/A snv 0.32 2
rs140685149
DEFB126
1.000 0.080 20 145670 frameshift variant CC/-;C;CCC delins 2
rs144944885
RPL23AP82 ; RABL2B
1.000 0.040 22 50776482 intron variant G/- delins 2
rs1555979575
MORC4 ; CLDN2
1.000 0.040 X 106928709 missense variant G/C snv 2
rs2276248
DNMT3L
1.000 0.040 21 44259375 intron variant T/C snv 6.1E-02 2
rs3819392
KIT
1.000 0.040 4 54660528 intron variant G/A snv 0.28 2
rs68073206
LHCGR ; STON1-GTF2A1L ; GTF2A1L
1.000 0.040 2 48721568 3 prime UTR variant A/C snv 0.29 2
rs864309485
TEX15
1.000 8 30846888 stop gained A/C snv 2
rs1042389
CYP2B6
19 41018248 3 prime UTR variant T/C snv 0.21 1
rs1050482
SLC20A1
2 112663757 3 prime UTR variant G/A snv 1
rs10841496
PDE3A
12 20368720 intron variant C/A snv 0.43 1
rs1259503 10 75232686 downstream gene variant C/G;T snv 1
rs1377547190
RAG1
11 36573327 missense variant C/T snv 1
rs1391383394
DNMT3B
20 32791692 missense variant T/C snv 7.0E-06 1
rs1399645
LOC105373644
2 139390262 intergenic variant C/T snv 9.0E-02 1