Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs259919
ZNRD1ASP
0.882 0.080 6 30057726 intron variant G/A snv 0.25 6
rs259940
ZNRD1ASP
0.925 0.080 6 30044157 intron variant A/G snv 0.23 2
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 15
rs2535238
ZFP57
1.000 0.080 6 29677261 5 prime UTR variant C/A;T snv 1
rs3747093
YDJC
0.732 0.200 22 21630090 upstream gene variant G/A snv 0.32 2
rs2131877
XXYLT1
0.827 0.080 3 195137645 intron variant G/A snv 0.20 1
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 9
rs12241008
VTI1A
0.716 0.160 10 112520943 intron variant T/C snv 0.13 9
rs7086803
VTI1A
0.763 0.160 10 112738717 intron variant G/A snv 0.20 4
rs5030807
VHL
0.851 0.320 3 10142113 missense variant T/A;C snv 5
rs1446876735
VHL
1.000 0.080 3 10142164 missense variant G/A snv 1
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs1105879
UGT1A9 ; UGT1A6 ; UGT1A7 ; UGT1A10 ; UGT1A8
0.790 0.240 2 233693556 missense variant A/C snv 0.35 0.34 2
rs2070959
UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A10 ; UGT1A6
0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 5
rs6759892
UGT1A6 ; UGT1A9 ; UGT1A7 ; UGT1A8 ; UGT1A10
0.851 0.160 2 233693023 missense variant T/G snv 0.39 0.39 3
rs371769427
U2AF1
0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06 9
rs7775397
TSBP1-AS1 ; TSBP1
0.790 0.400 6 32293475 missense variant T/G snv 6.0E-02 6.4E-02 7
rs3817963
TSBP1-AS1 ; BTNL2
0.776 0.360 6 32400310 intron variant T/C snv 0.25 5
rs2523989
TRIM31 ; TRIM31-AS1
0.827 0.280 6 30110498 missense variant C/T snv 0.12 0.12 5
rs2517598
TRIM31 ; TRIM31-AS1
0.851 0.280 6 30112497 synonymous variant G/A snv 0.14 0.13 4
rs2523987
TRIM31-AS1 ; TRIM31
0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 5
rs2257914
TRIM10
0.925 0.200 6 30152786 3 prime UTR variant C/A snv 0.17 2
rs13314271
TP63
0.925 0.080 3 189639813 intron variant T/C snv 0.45 2
rs4488809
TP63
0.827 0.080 3 189638472 intron variant T/C snv 0.45 2
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 1