Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 1
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs7597593
ZNF804A
0.827 0.160 2 184668853 intron variant T/C snv 0.53 6
rs12476147
ZNF804A
0.851 0.040 2 184936178 missense variant A/T snv 0.66 0.59 4
rs13423388
ZNF804A
1.000 0.040 2 184915498 intron variant G/A snv 0.15 1
rs1366842
ZNF804A
1.000 0.040 2 184937516 missense variant C/A;T snv 0.59; 4.1E-06 1
rs359895
ZNF804A ; LOC105373780
1.000 0.040 2 184598458 non coding transcript exon variant T/A snv 0.57 1
rs3731834
ZNF804A
1.000 0.040 2 184938637 missense variant C/G snv 0.17 0.14 1
rs56280129
ZNF804A
1.000 0.040 2 184915579 intron variant G/A snv 5.8E-04 1
rs61739290
ZNF804A
1.000 0.040 2 184936870 missense variant A/G snv 5.4E-02 5.4E-02 1
rs749914296
ZNF569
1.000 0.040 19 37413561 missense variant A/G snv 4.0E-06 1
rs2053079
ZNF536
1.000 0.040 19 30496516 intron variant A/G snv 0.19 1
rs1233710
ZKSCAN4
1.000 0.040 6 28247668 intron variant C/T snv 0.13 1
rs2235359
ZKSCAN4
0.925 0.160 6 28247863 intron variant T/G snv 0.20 1
rs12991836
ZEB2
1.000 0.040 2 144383974 intron variant A/C;T snv 1
rs6755392
ZEB2
1.000 0.040 2 144484555 intron variant A/G snv 0.60 1
rs175174
ZDHHC8
0.882 0.120 22 20140031 non coding transcript exon variant A/G snv 0.44 3
rs3803300
ZBTB42
0.827 0.120 14 104803442 3 prime UTR variant T/A;C snv 6
rs9841504
ZBTB20
0.827 0.120 3 114643917 intron variant C/G;T snv 6
rs28365859
YWHAE
1.000 0.040 17 1400484 upstream gene variant C/G snv 0.38 1
rs35268
XRCC4
1.000 0.040 5 83292677 intron variant T/C snv 0.18 1
rs6452536
XRCC4
1.000 0.040 5 83249564 intron variant C/A;G snv 1
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs17551608
WWC1
1.000 0.040 5 168408534 missense variant C/T snv 0.12 0.11 1