Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11662595
HRH4
0.882 0.120 18 24477006 missense variant A/G snv 8.6E-02 7.6E-02 7
rs7240004 1.000 0.040 18 48868651 intergenic variant A/G snv 0.43 4
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs2333227
MPO
0.752 0.320 17 58281401 upstream gene variant C/T snv 0.24 15
rs8179090
TIMP2
0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02 12
rs121917887
NME1-NME2 ; NME1
0.790 0.120 17 51161744 missense variant A/G snv 6.0E-05 7.0E-05 10
rs1064793929
TP53
0.882 0.280 17 7675167 frameshift variant A/-;AA delins 5
rs61552325
ERBB2
0.882 0.080 17 39727784 missense variant C/G snv 5
rs141613848
SLC9A3R1
0.925 0.080 17 74768481 missense variant A/T snv 1.0E-03 1.2E-03 4
rs877610
TRPV1
1.000 17 3572196 synonymous variant C/T snv 4.6E-02 7.5E-02 3
rs12918952
WWOX
0.851 0.120 16 78386878 missense variant G/A;C;T snv 7
rs587782359
CDH1
1.000 0.080 16 68812244 missense variant C/G;T snv 2.8E-05 3
rs1022088103
MMP2
16 55485759 missense variant G/A snv 1
rs1231584616
MMP2
16 55485367 missense variant G/A snv 4.0E-06 1
rs774390402
BCAR1
16 75235116 missense variant A/C snv 1.2E-05 1
rs1478604
THBS1
0.807 0.240 15 39581120 5 prime UTR variant T/C snv 0.40 9
rs1057519906
IDH2
0.882 0.120 15 90088607 missense variant T/A;C snv 8
rs35697691
LOC112268150 ; MAPK6
15 52061301 missense variant C/G snv 5.8E-02 5.9E-02 3
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs763538721
HIF1A-AS3 ; HIF1A
0.807 0.160 14 61740897 missense variant T/A snv 4.0E-06 8