Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs324125
ZNF880
19 52384029 missense variant A/G snv 0.13 0.16 1
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs12932445
ZFHX3
0.925 0.080 16 73035989 intron variant T/C snv 0.18 3
rs879324
ZFHX3
1.000 0.080 16 73034779 intron variant G/A snv 0.17 2
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs12037987
WNT2B
1 112500200 intron variant T/C snv 8.6E-02 2
rs7582720
WDR12
1.000 0.040 2 202888349 intron variant T/C snv 8.9E-02 2
rs17771318
WDFY4
10 48703312 intron variant G/A snv 2.9E-02 1
rs2359612
VKORC1
0.851 0.120 16 31092475 intron variant A/G snv 0.66 7
rs61742245
VKORC1
16 31094624 missense variant C/A;T snv 2.4E-03 2
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs752907384
VEGFA
0.827 0.200 6 43782077 missense variant C/G;T snv 8.0E-06 6
rs3783613
VCAM1
0.851 0.200 1 100731231 missense variant G/A;C snv 4.0E-06; 9.9E-03 6
rs1010
VAMP8
0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
rs6742078
UGT1A3 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A6 ; UGT1A4 ; UGT1A9 ; UGT1A1 ; UGT1A5
0.807 0.240 2 233763993 intron variant G/T snv 0.36 13
rs145067756
UBE2Z
17 48923631 intron variant -/AAACAATGTCACAG;AAAGAATGTCACAG;AAAGAATGTCGCAG;AATGTCACAG;AGAGAATGTCACAG delins 0.40 1
rs77149783
UBE2Z
17 48923631 intron variant A/C;T snv 1
rs7260579
TULP2
19 48897377 missense variant C/T snv 0.15 0.18 1
rs463312
TUBB1
1.000 0.040 20 59022915 missense variant A/C snv 7.7E-02 5.7E-02 4
rs1234442507
TUBB1
1.000 0.040 20 59022915 frameshift variant AG/- del 4.0E-06 3
rs2632512
TSPOAP1-AS1 ; RNF43
17 58374461 intron variant T/C snv 0.85 1
rs17490626
TSPAN15
0.882 0.120 10 69458890 intron variant G/C snv 8.4E-02 5