Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs10888690
FAF1
0.807 0.080 1 50494849 intron variant T/A;C snv 7
rs111668293
TBX15
0.807 0.080 1 118896200 intron variant G/- del 0.12 7
rs12083887 0.807 0.080 1 118339066 regulatory region variant A/G snv 0.62 7
rs12565727
C1orf127
0.807 0.080 1 10973025 intron variant A/G snv 0.31 7
rs2095921
C1orf127
0.807 0.080 1 10973265 intron variant C/G;T snv 7
rs7534070 0.807 0.080 1 25171684 intergenic variant G/A;T snv 7
rs7542354
C1orf127
0.807 0.080 1 10980328 intron variant G/A snv 0.37 7
rs78003935 0.807 0.080 1 170372381 upstream gene variant T/A;G snv 0.25 7
rs111238176
FASLG
0.851 0.160 1 172665840 missense variant A/G snv 4
rs1005734
LOC105376878 ; RUNX3
1.000 0.080 1 24935531 intron variant C/A;T snv 1
rs10903128 1.000 0.080 1 25036847 upstream gene variant A/G snv 0.68 1
rs10919382 1.000 0.080 1 170392023 intergenic variant A/G snv 0.36 1
rs115176171 1.000 0.080 1 25006643 intergenic variant A/G snv 6.7E-02 1
rs115282290 1.000 0.080 1 204009986 downstream gene variant C/G;T snv 1
rs11586871 1.000 0.080 1 25073178 intron variant C/T snv 0.15 1
rs116315504
ZC3H11A ; ZBED6
1.000 0.080 1 203820951 intron variant C/G;T snv 1
rs12077761 1.000 0.080 1 25082765 intron variant A/G snv 0.21 1
rs12123537
ZBED6 ; ZC3H11A
1.000 0.080 1 203822046 intron variant C/G;T snv 1
rs12144907
PUDPP2
1.000 0.080 1 152145741 intron variant G/C;T snv 1
rs12745121 1.000 0.080 1 25141389 regulatory region variant G/A snv 0.23 1
rs142020459
PEX14
1.000 0.080 1 10512026 intron variant C/G snv 1.8E-02 1
rs143916866
SRRM1
1.000 0.080 1 24641046 intron variant C/T snv 1.0E-02 1
rs1576101 1.000 0.080 1 40901526 intergenic variant A/T snv 0.31 1