Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1003129577
WDR48
3 39094706 missense variant G/C snv 1
rs10046
MIR4713HG ; CYP19A1
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43 18
rs10053538
HAVCR2
0.807 0.160 5 157110499 intron variant C/A;T snv 7
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10074991
PRKAA1
0.851 0.120 5 40790449 intron variant G/A snv 0.31 7
rs1007541
FSHR
0.882 0.080 2 48981895 intron variant C/T snv 0.16 4
rs10079250
CSF1R
0.827 0.120 5 150070569 missense variant T/C snv 9.9E-02 8.6E-02 7
rs10090154 0.807 0.160 8 127519892 intergenic variant T/A;C snv 7
rs1010898370
IDH1
1.000 2 208243469 missense variant T/C;G snv 8.0E-06 2
rs1011329790
GGCT
0.925 0.080 7 30504681 missense variant G/A snv 3
rs1012477
PER3
0.827 0.160 1 7798075 intron variant G/C snv 0.16 8
rs1014509103
ADAMTS4
1.000 0.080 1 161194005 missense variant G/A snv 4.0E-06 2.8E-05 2
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs1017621656
TGFB1
0.925 0.080 19 41352923 missense variant A/C;G snv 1.9E-05 3
rs10204525
PDCD1
0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs1020833107
TTF1
9 132398145 synonymous variant G/A snv 7.0E-06 1
rs10235235
ZNF394 ; ZNF789
0.925 0.080 7 99478208 intron variant T/C snv 0.13 4
rs1024708183
MAP2K7
0.925 0.040 19 7909761 missense variant A/G snv 4
rs10269422
HDAC9
7 18814978 intron variant T/A snv 0.46 1
rs1029342144
KLLN ; PTEN
0.882 0.120 10 87864162 5 prime UTR variant C/G;T snv 6
rs1034749666
OLIG2
0.776 0.160 21 33027257 missense variant G/A snv 9
rs1040264140
FURIN
1.000 0.080 15 90881744 missense variant A/G snv 2
rs1041326
DAPK1
9 87541931 intron variant C/T snv 0.14 1
rs1042028
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs1042489
BIRC5
0.851 0.160 17 78224125 3 prime UTR variant T/C snv 0.40 5