Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12704795
rs12704795
PON2
1 1.000 0.080 7 95424695 intron variant T/G snv 0.34 0.010 1.000 1 2006 2006
dbSNP: rs17319721
rs17319721
SHROOM3
5 0.925 0.080 4 76447694 intron variant G/A snv 0.34 0.010 1.000 1 2017 2017
dbSNP: rs367825197
rs367825197
PODXL
2 0.925 0.080 7 131509412 stop gained G/A snv 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs538166970
rs538166970
ACE
2 0.925 0.080 17 63496920 missense variant G/A;C snv 1.6E-05; 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs867394500
rs867394500
ACE
4 0.851 0.080 17 63477301 missense variant G/T snv 0.010 1.000 1 2003 2003
dbSNP: rs1567202189
rs1567202189
PKD1
2 1.000 0.080 16 2111276 inframe insertion -/GTG ins 0.700 0
dbSNP: rs530391015
rs530391015
INF2
5 0.882 0.080 14 104703445 stop gained G/A;C;T snv 4.0E-06 0.700 0
dbSNP: rs7222094
rs7222094
MAP3K14
3 0.882 0.120 17 45290287 intron variant T/C snv 0.54 0.010 1.000 1 2011 2011
dbSNP: rs7456421
rs7456421
HIPK2
4 0.882 0.120 7 139715976 synonymous variant G/C snv 0.27 0.37 0.010 < 0.001 1 2013 2013
dbSNP: rs1553948516
rs1553948516
SCARB2
3 0.925 0.120 4 76181009 frameshift variant -/G delins 0.700 0
dbSNP: rs1382048442
rs1382048442
ABCC2
2 0.925 0.160 10 99797141 missense variant T/C snv 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs138207257
rs138207257
HOGA1
2 0.925 0.160 10 97611535 missense variant G/A;T snv 2.0E-05; 1.1E-04 0.010 1.000 1 2017 2017
dbSNP: rs202047589
rs202047589
HOGA1
2 0.925 0.160 10 97599780 missense variant C/T snv 4.4E-05 7.0E-05 0.010 1.000 1 2017 2017
dbSNP: rs281874657
rs281874657
COL4A5
3 0.925 0.160 X 108586717 stop gained C/T snv 0.010 1.000 1 2017 2017
dbSNP: rs886039813
rs886039813
OFD1
8 0.827 0.160 X 13756600 frameshift variant C/- delins 0.700 0
dbSNP: rs188942711
rs188942711
COL4A3 ; MFF-DT
9 0.763 0.200 2 227253336 missense variant G/A;T snv 2.8E-05; 4.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs118203478
rs118203478
TSC1
5 0.882 0.200 9 132911492 frameshift variant -/A;AA delins 0.700 0
dbSNP: rs12026
rs12026
PON2
6 0.827 0.240 7 95411704 missense variant G/C snv 0.27 0.27 0.010 1.000 1 2006 2006
dbSNP: rs34557412
rs34557412
TNFRSF13B
15 0.763 0.240 17 16948873 missense variant A/G snv 3.5E-03 3.9E-03 0.010 1.000 1 2006 2006
dbSNP: rs61747728
rs61747728
NPHS2
20 0.701 0.240 1 179557079 missense variant C/T snv 3.0E-02 2.8E-02 0.010 1.000 1 2008 2008
dbSNP: rs1555487316
rs1555487316
UMOD
5 0.882 0.240 16 20348247 missense variant A/C snv 0.700 0
dbSNP: rs771454167
rs771454167
CEP290
6 0.827 0.240 12 88062772 frameshift variant C/- del 4.7E-05; 5.2E-06 2.1E-05 0.700 0
dbSNP: rs121918079
rs121918079
TTR
10 0.790 0.280 18 31595143 missense variant T/C snv 0.010 1.000 1 2017 2017
dbSNP: rs74315289
rs74315289
BSND
5 0.827 0.280 1 54999325 missense variant G/A snv 1.0E-04 1.5E-04 0.010 1.000 1 2011 2011
dbSNP: rs137852832
rs137852832
CEP290
17 0.716 0.280 12 88077263 stop gained C/A snv 9.5E-05 6.3E-05 0.700 0