Source: CURATED ×
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 38
rs12150079
ZPBP2
0.807 0.280 17 39869164 intron variant G/A snv 0.24 1
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 8
rs1343795
ZNF652
0.882 0.120 17 49334880 intron variant C/A snv 0.78 1
rs7225787
ZNF652
17 49351211 intron variant A/C snv 0.43 1
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs3747093
YDJC
0.732 0.200 22 21630090 upstream gene variant G/A snv 0.32 2
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 1
rs2294693
UNC5CL ; OARD1
1.000 0.080 6 41037763 intron variant T/C snv 0.26 1
rs10929251
UGT1A10 ; UGT1A8
1.000 0.080 2 233637583 intron variant A/G snv 0.13 2
rs17864678
UGT1A10 ; UGT1A8
1.000 0.080 2 233635964 intron variant T/A snv 5.6E-03 2
rs1395602
UBN1
16 4861238 intron variant A/C snv 0.55 1
rs2251666
UBN1
16 4873090 intron variant G/A;C snv 0.37; 4.0E-06 1
rs6500637
UBN1
16 4870660 intron variant T/C snv 0.39; 4.0E-06 0.40 1
rs8064029
UBN1
16 4863368 intron variant C/T snv 0.13 1
rs371769427
U2AF1
0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06 9
rs371246226
U2AF1
0.827 0.160 21 43094667 missense variant T/C;G snv 2.4E-05; 2.4E-05 2
rs2076530
TSBP1-AS1 ; BTNL2
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 6
rs4987668
TRPV6
7 142874896 splice region variant A/G snv 9.0E-02 0.20 1
rs4252381
TRPV5
7 142932278 intron variant G/T snv 0.23 1
rs4252416
TRPV5
7 142928322 intron variant C/A;G;T snv 1
rs4252435
TRPV5
7 142925619 synonymous variant A/G;T snv 1
rs6968949
TRBVA
7 142681544 intron variant C/T snv 0.53 1
rs17251
TRBV27
0.925 0.120 7 142715462 intron variant C/A snv 0.33 0.37 3