Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11031005
LOC105376607
1.000 0.120 11 30204809 intron variant T/C snv 0.10 5
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
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
rs1038822
THADA
1.000 0.120 2 43511034 intron variant T/A;C snv 1
rs1044386
FEM1A
1.000 0.120 19 4795277 3 prime UTR variant G/A snv 0.20 1
rs1045435
PMEL ; RAB5B ; CDK2
1.000 0.120 12 55972376 3 prime UTR variant G/C snv 0.15 1
rs10459247
HSD17B6
1.000 0.120 12 56777732 intron variant T/C snv 0.21 1
rs10495960
GTF2A1L ; STON1-GTF2A1L ; LHCGR
1.000 0.120 2 48732893 missense variant G/A snv 0.18 0.14 1
rs10505648
LINC02055
1.000 0.120 8 136144207 intron variant A/G snv 0.43 1
rs10514258
VCAN-AS1 ; VCAN
1.000 0.120 5 83575938 intron variant A/G snv 0.13 1
rs1056917
RUVBL2 ; LHB
1.000 0.120 19 49016209 synonymous variant A/G snv 0.61 0.65 1
rs1062809
FST
1.000 0.120 5 53484261 missense variant C/A;G snv 1
rs10739076 1.000 0.120 9 5440589 upstream gene variant A/C;T snv 1