Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11892031
UGT1A10 ; UGT1A8
0.882 0.120 2 233656637 intron variant A/C;T snv 4
rs1014971 0.882 0.120 22 38936618 regulatory region variant C/T snv 0.55 2
rs10775480
LOC105372093 ; SLC14A1
0.882 0.120 18 45737317 intron variant T/C snv 0.61 2
rs17674580
SLC14A1 ; LOC105372093
0.882 0.120 18 45729946 5 prime UTR variant C/A;T snv 2
rs798766
TACC3
0.851 0.120 4 1732512 intron variant T/C snv 0.76 2
rs8102137 0.882 0.120 19 29805946 regulatory region variant T/C snv 0.24 2
rs11543198
CLK3
0.882 0.120 15 74619987 missense variant G/A;T snv 0.11 1
rs118203347
TSC1
1.000 0.120 9 132927208 missense variant T/C snv 7.0E-06 1
rs118203385
TSC1
1.000 0.120 9 132923383 missense variant A/C;G snv 1
rs1323541164
TSC1
1.000 0.120 9 132921834 missense variant A/C snv 1
rs2042329
CWC27
0.882 0.120 5 64771925 intron variant T/C;G snv 1
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs1046778
AS3MT ; BORCS7-ASMT ; LOC107984265
0.851 0.160 10 102901727 3 prime UTR variant T/C snv 0.30 1
rs710521 0.851 0.200 3 189928144 intergenic variant T/C snv 0.24 3
rs786204929
PTEN
0.752 0.200 10 87933144 stop gained G/A;T snv 3
rs2293607
TERC
0.807 0.200 3 169764547 non coding transcript exon variant T/A;C snv 2
rs13278062
LOC389641 ; TNFRSF10A
0.807 0.200 8 23225458 non coding transcript exon variant G/A;C;T snv 1
rs138213197
HOXB13
0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 8
rs1495741 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 6
rs28931615
FGFR3
0.732 0.240 4 1804426 missense variant C/A;T snv 3
rs9642880
CASC11
0.776 0.240 8 127705823 intron variant G/A;T snv 3
rs760805
RUNX3 ; LOC107984932
0.776 0.240 1 24925432 intron variant A/T snv 0.42 2
rs2067079
GAS5 ; SNORA103 ; SNORD80 ; SNORD77 ; SNORD81 ; SNORD44 ; SNORD78 ; SNORD47 ; SNORD79
0.807 0.240 1 173866073 non coding transcript exon variant C/T snv 0.22 0.18 1
rs2230641
CCNH
0.807 0.240 5 87399457 missense variant A/G;T snv 0.18 0.17 1
rs3731239
CDKN2A
0.763 0.240 9 21974219 intron variant A/G snv 0.26 1