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: rs4821481
rs4821481
MYH9
1 1.000 0.080 22 36299896 intron variant C/T snv 0.78 0.010 1.000 1 2009 2009
dbSNP: rs4961
rs4961
ADD1
27 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.010 1.000 1 2006 2006
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: 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 2012 2012
dbSNP: rs662
rs662
PON1
157 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2010 2010
dbSNP: rs699
rs699
AGT
134 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2003 2003
dbSNP: rs734553
rs734553
SLC2A9
7 0.851 0.240 4 9921380 intron variant G/A;T snv 0.010 1.000 1 2015 2015
dbSNP: rs754919065
rs754919065
TRPC6
1 1.000 0.080 11 101504767 missense variant G/A snv 6.1E-05; 4.1E-06 7.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs7582694
rs7582694
STAT4
9 0.763 0.400 2 191105394 intron variant C/G snv 0.77 0.010 1.000 1 2013 2013
dbSNP: rs760336723
rs760336723
PODXL
3 0.882 0.240 7 131506292 missense variant G/A snv 2.8E-05 5.6E-05 0.010 1.000 1 2004 2004
dbSNP: rs867394500
rs867394500
ACE
4 0.851 0.080 17 63477301 missense variant G/T snv 0.010 1.000 1 2003 2003