Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10033366
ENPEP
4 110409934 intron variant T/C snv 0.92 1
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 1
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 8
rs10050860
ERAP1
0.882 0.240 5 96786506 missense variant C/T snv 0.15 0.16 1
rs10069554 5 33204354 intron variant T/C snv 0.45 1
rs10184428 2 164155317 intron variant C/A;G snv 5
rs10188442
GPR39
2 132431666 intron variant C/T snv 0.22 1
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 10
rs1027989
LYN
8 55901862 intron variant G/A;C snv 3
rs10279895 7 27288591 intergenic variant A/G snv 2.9E-02 1
rs104886142
COL4A5
0.790 0.280 X 108598793 missense variant G/A snv 8.7E-05 4.7E-05 4
rs104893831
VHL
0.925 0.040 3 10146549 missense variant G/A;C;T snv 2.0E-05 2
rs104893914
NR3C1
1.000 0.080 5 143282714 missense variant C/T snv 1
rs104894145
CYP17A1-AS1 ; CYP17A1 ; WBP1L
0.925 0.240 10 102830946 missense variant G/A snv 1
rs10496288 2 83065441 intergenic variant T/C snv 0.13 1
rs10496289 2 83066256 intergenic variant C/T snv 0.13 1
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 11
rs1057518797
PKD2
4 88008090 frameshift variant CCCGGGCA/TAGGACG delins 3
rs1057518856
PKD1
0.882 0.240 16 2102397 missense variant A/T snv 5
rs1057518897
PKD1
0.925 0.120 16 2103746 missense variant C/T snv 7.0E-06 3
rs1057518899
PKD1
16 2111647 stop gained G/A snv 2
rs1057518903
MEN1
0.882 0.160 11 64807890 splice region variant C/- delins 6
rs1057518959
PKD1 ; MIR1225 ; LOC105371049
16 2091794 missense variant A/G snv 2
rs1057523354
COL4A1
0.763 0.480 13 110179387 missense variant C/A snv 13
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 7