Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs826220
THRB
1.000 0.040 3 24227186 intron variant C/T snv 0.70 1
rs121912683
SLC25A4
0.851 0.200 4 185145020 missense variant C/A snv 4.0E-06 7.0E-06 9
rs10033900
CFI
0.807 0.040 4 109737911 intron variant T/C snv 0.54 7
rs10034228 0.882 0.040 4 111690594 intergenic variant T/C snv 0.32 3
rs13129838
OR7E94P ; LINC00989 ; LOC107986294
1.000 0.040 4 79587634 non coding transcript exon variant T/C snv 0.66 1
rs1585471 1.000 0.040 4 111781479 regulatory region variant A/G snv 0.30 1
rs2218817 1.000 0.040 4 111689850 regulatory region variant G/A snv 0.32 1
rs5022942
BMP3
1.000 0.040 4 81038812 intron variant A/G snv 0.59 1
rs6837348 1.000 0.040 4 111787647 intergenic variant G/A snv 0.28 1
rs12716080
CTNND2
0.882 0.040 5 11166836 intron variant G/T snv 0.39 3
rs6885224
CTNND2
0.882 0.040 5 11169833 intron variant C/A;T snv 3
rs2973644
FGF10
0.925 0.040 5 44384081 intron variant C/A;T snv 2
rs339501
FGF10
0.925 0.040 5 44365531 intron variant C/T snv 0.94 2
rs79002828
FGF10
0.925 0.040 5 44318015 intron variant A/G snv 9.6E-03 2
rs10462070
FGF10
1.000 0.040 5 44305647 intron variant A/G snv 1.2E-02 1
rs11743810
EGR1
1.000 0.040 5 138466715 intron variant C/T snv 0.50 0.48 1
rs12517396
FGF10
1.000 0.040 5 44359424 intron variant C/A snv 4.1E-02 1
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1554208945
ZNF292
0.752 0.240 6 87260207 missense variant A/C snv 26
rs1562127631
IRAK1BP1 ; PHIP
0.742 0.360 6 78961751 frameshift variant C/- del 24
rs387907141
ARID1B
0.752 0.360 6 157181137 stop gained C/T snv 24
rs1554210073
PHIP
0.752 0.320 6 79042844 frameshift variant GT/A delins 21
rs1327062642
TULP1
0.827 0.200 6 35509903 frameshift variant -/G delins 4.0E-06 11
rs876657380
ARID1B
0.851 0.360 6 157181155 frameshift variant AA/- delins 11
rs755604487
PHIP
0.790 0.200 6 79026079 stop gained G/A;C snv 10