Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1058261
DES
2 219420587 synonymous variant C/T snv 0.33 0.37 2
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1061376
FBLN2
3 13637835 missense variant C/G;T snv 0.37 0.41 1
rs1065297
CXCL12
0.925 0.040 10 44370528 3 prime UTR variant A/G snv 5.4E-02 3
rs10719
DROSHA
0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs10737175 1 159750152 intergenic variant T/C snv 0.24 1
rs10738554
SLC24A2
9 19904105 intergenic variant T/C snv 0.46 1
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10745332
CAPZA1
1 112646431 intron variant G/A snv 0.77 3
rs10754558
NLRP3
0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10759931 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 9
rs10770141
MIR4686 ; TH
1.000 0.120 11 2172610 upstream gene variant A/C;G snv 2
rs10776752
WNT2B
1 112501706 intron variant G/T snv 8.8E-02 4
rs1078499
AGT
1 230713350 intron variant A/G snv 0.30 1
rs10785581
LOC105369743
12 45537190 intron variant C/A;G snv 1
rs10792367
SLC22A8
11 62991327 non coding transcript exon variant C/G snv 0.44 1
rs10793538
CXCL12
1.000 0.040 10 44381138 intron variant T/A;C snv 2