Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10811474 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 11
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs11077654
SLC39A11
0.882 0.120 17 73010373 intron variant A/C snv 0.69 3
rs1109324 0.827 0.160 6 43762018 intergenic variant G/T snv 0.15 5
rs11191438
AS3MT ; BORCS7-ASMT
0.882 0.120 10 102878107 intron variant G/A;C snv 3
rs11191439
AS3MT ; BORCS7-ASMT
0.851 0.120 10 102878966 missense variant T/A;C snv 9.2E-02 6
rs11191454
LOC107984265 ; BORCS7-ASMT ; AS3MT
0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 9
rs11249206
RUNX3 ; LOC105376878
0.851 0.160 1 24951491 intron variant C/T snv 0.48 4
rs1130214
AKT1
0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs1130233
AKT1
0.742 0.480 14 104773557 synonymous variant C/T snv 0.30 0.23 13
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1135612
POR
0.882 0.120 7 75980359 synonymous variant A/G;T snv 0.28 3
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1141718
SOD2
0.724 0.280 6 159688224 missense variant A/G snv 15
rs11466445
TGFBR1
0.851 0.160 9 99105256 inframe insertion GCGGCGGCGGCGGCG/-;GCG;GCGGCG;GCGGCGGCG;GCGGCGGCGGCG;GCGGCGGCGGCGGCGGCG;GCGGCGGCGGCGGCGGCGGCG;GCGGCGGCGGCGGCGGCGGCGGCG;GCGGCGGCGGCGGCGGCGGCGGCGGCG delins 5
rs11543198
CLK3
0.882 0.120 15 74619987 missense variant G/A;T snv 0.11 3
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11671784
MIR24-2 ; LOC284454 ; MIR23A ; MIR27A
0.790 0.240 19 13836482 non coding transcript exon variant G/A snv 1.2E-02 1.2E-02 9
rs11685387
XRCC5
0.776 0.240 2 216109091 splice region variant C/T snv 0.30 9
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
rs11871756
SLC39A11
0.882 0.120 17 72730105 intron variant C/G snv 0.11 3
rs11892031
UGT1A10 ; UGT1A8
0.882 0.120 2 233656637 intron variant A/C;T snv 5