Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11031006
LOC105376607
0.882 0.120 11 30204981 intron variant G/A snv 0.11 8
rs7759938
LIN28B-AS1
0.925 0.120 6 104931079 intron variant C/T snv 0.62 7
rs11031005
LOC105376607
1.000 0.120 11 30204809 intron variant T/C snv 0.10 5
rs11668344
TMEM150B
0.925 0.120 19 55322296 intron variant A/G snv 0.35 4
rs184752888
BRD2
0.882 0.120 6 32977847 missense variant G/A snv 4
rs2479106
DENND1A
0.851 0.120 9 123762933 intron variant A/G snv 0.44 4
rs2252673
INSR
0.882 0.120 19 7150407 intron variant C/G snv 0.75 3
rs7371084
GTF2A1L ; LHCGR ; STON1-GTF2A1L
0.925 0.120 2 48712814 intron variant T/C snv 0.12 3
rs772920
SUOX ; RAB5B
0.925 0.120 12 55996580 3 prime UTR variant C/G;T snv 3
rs112137861
SOX5
1.000 0.120 12 23857104 intron variant C/A snv 3.3E-02 2
rs11889798
C2orf83 ; LOC729968
1.000 0.120 2 227616703 intron variant C/T snv 0.13 2
rs140485756 1.000 0.120 6 69410439 intergenic variant T/C snv 3.2E-02 2
rs1999805
ESR1
1.000 0.120 6 151747229 intron variant G/A snv 0.55 2
rs2252281
SLC47A1
1.000 0.120 17 19533874 5 prime UTR variant T/C snv 0.32 2
rs2910397 1.000 0.120 19 47894860 intergenic variant C/T snv 0.38 2
rs56949836 1.000 0.120 9 90167763 intergenic variant C/T snv 8.9E-02 2
rs71361504
BRCA1 ; NBR2
0.925 0.120 17 43125988 intron variant -/GTT delins 2
rs7312770 0.925 0.120 12 56073803 upstream gene variant C/T snv 0.53 2
rs74585555 1.000 0.120 2 81214976 intergenic variant G/A snv 4.9E-02 2
rs76169311
CRB1
1.000 0.120 1 197372771 intron variant G/A snv 0.13 2
rs7766109
F13A1
1.000 0.120 6 6256600 intron variant G/A snv 0.63 2
rs8108622
INSR
1.000 0.120 19 7182742 intron variant T/A snv 0.23 2
rs877636
ERBB3
1.000 0.120 12 56086799 intron variant G/A snv 0.61 2
rs10152450
FEM1B
1.000 0.120 15 68279141 intron variant T/G snv 0.34 1
rs10179648
THADA
1.000 0.120 2 43580926 intron variant C/T snv 0.70 1