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: rs1045485
rs1045485
34 0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 0.020 1.000 2 2009 2016
dbSNP: rs1035938
rs1035938
8 0.776 0.120 19 47680514 missense variant C/G;T snv 0.29 0.010 1.000 1 2010 2010
dbSNP: rs2235544
rs2235544
14 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs267606541
rs267606541
AIP
5 0.827 0.160 11 67487147 stop gained C/T snv 0.010 1.000 1 2012 2012
dbSNP: rs2686876
rs2686876
3 0.882 0.080 11 258909 intergenic variant T/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs3219466
rs3219466
4 0.851 0.080 1 45340381 5 prime UTR variant G/A;T snv 0.010 1.000 1 2010 2010
dbSNP: rs3731249
rs3731249
23 0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02 0.010 1.000 1 2019 2019
dbSNP: rs397507444
rs397507444
306 0.405 0.880 1 11794407 missense variant T/G snv 0.010 1.000 1 2017 2017
dbSNP: rs603965
rs603965
14 0.732 0.440 11 69648142 splice region variant G/A snv 0.010 1.000 1 2019 2019
dbSNP: rs730882035
rs730882035
VHL
7 0.807 0.200 3 10149805 missense variant G/A snv 0.010 1.000 1 2006 2006
dbSNP: rs768803947
rs768803947
3 0.882 0.080 17 7670624 missense variant C/A;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2001 2001
dbSNP: rs854560
rs854560
113 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 0.010 1.000 1 2010 2010
dbSNP: rs9420907
rs9420907
7 0.790 0.320 10 103916707 intron variant C/A;G snv 0.010 1.000 1 2019 2019
dbSNP: rs1217691063
rs1217691063
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs150766139
rs150766139
13 0.742 0.320 16 2046238 stop gained G/A snv 1.4E-03 1.4E-03 0.010 1.000 1 2019 2019
dbSNP: rs1800067
rs1800067
17 0.716 0.320 16 13935176 missense variant G/A snv 5.6E-02 5.3E-02 0.010 1.000 1 2010 2010
dbSNP: rs4968451
rs4968451
13 0.732 0.160 17 61849946 intron variant A/C snv 0.15 0.020 1.000 2 2008 2018
dbSNP: rs10936599
rs10936599
32 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 0.010 1.000 1 2019 2019
dbSNP: rs1243180
rs1243180
7 0.790 0.160 10 21626690 intron variant T/A snv 0.23 0.010 1.000 1 2015 2015
dbSNP: rs12770228
rs12770228
4 0.882 0.080 10 21494705 non coding transcript exon variant G/A snv 0.24 0.020 1.000 2 2015 2017
dbSNP: rs1801131
rs1801131
93 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 0.020 1.000 2 2017 2017
dbSNP: rs1805794
rs1805794
NBN
41 0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 0.010 1.000 1 2010 2010
dbSNP: rs11012732
rs11012732
5 0.882 0.080 10 21541175 intron variant A/G snv 0.31 0.010 1.000 1 2011 2011
dbSNP: rs25406
rs25406
8 0.807 0.120 20 5118990 intron variant G/A snv 0.41 0.010 1.000 1 2010 2010
dbSNP: rs7574920
rs7574920
XDH
3 0.882 0.080 2 31362783 intron variant G/C snv 0.42 0.010 1.000 1 2009 2009