Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4806213
NPHS1
1.000 0.080 19 35831699 missense variant T/C snv 9.7E-02 0.11 1
rs748203170
AXDND1 ; NPHS2
1.000 0.080 1 179551346 missense variant G/A snv 8.0E-06 1
rs920479356
NPHS2
1.000 0.080 1 179575836 missense variant C/G;T snv 1
rs74315342
NPHS2
0.763 0.120 1 179561327 missense variant C/T snv 6.0E-04 5.3E-04 10
rs71785313
APOL1
0.882 0.120 22 36265996 inframe deletion TTATAA/- delins 5
rs267602852
WT1
0.827 0.160 11 32417631 missense variant G/A snv 7
rs75462234
PAX2
0.851 0.160 10 100749772 frameshift variant G/-;GG;GGG delins 4
rs1799937
WT1
0.882 0.160 11 32389228 intron variant A/G snv 0.35 0.35 3
rs2301254
WT1-AS ; WT1
0.882 0.160 11 32436129 intron variant A/G snv 0.48 3
rs6508
WT1-AS
0.882 0.160 11 32438918 non coding transcript exon variant G/A snv 8.3E-02 0.16 3
rs188942711
COL4A3 ; MFF-DT
0.763 0.200 2 227253336 missense variant G/A;T snv 2.8E-05; 4.0E-06 9
rs61747728
NPHS2
0.701 0.240 1 179557079 missense variant C/T snv 3.0E-02 2.8E-02 20
rs748106387
SMARCAL1
0.851 0.240 2 216415427 stop gained C/A;T snv 2.8E-05 9
rs2239785
APOL1
0.827 0.240 22 36265284 missense variant G/A snv 0.79 0.68 5
rs267607555
LMNA
0.807 0.280 1 156136009 missense variant C/T snv 7.0E-06 6
rs1422329310
PLCE1
0.925 0.280 10 94265844 synonymous variant G/A snv 4.0E-06 2
rs119473033
SMARCAL1
0.827 0.320 2 216478216 stop gained G/T snv 8.0E-05 1.3E-04 11
rs140511594
TTC21B ; TTC21B-AS1
0.742 0.360 2 165941111 missense variant G/A snv 1.3E-04 1.1E-04 13
rs866294686
TRIM8 ; LOC105378460
0.683 0.480 10 102657073 stop gained C/A;T snv 43
rs5742909
CTLA4
0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1800471
TGFB1
0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48