Source: GWASDB ×
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: rs10903122
rs10903122
5 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 0.700 1.000 2 2011 2011
dbSNP: rs11778371
rs11778371
1 1.000 0.080 8 27462388 intron variant C/T snv 4.0E-02 0.700 1.000 2 2009 2010
dbSNP: rs12150079
rs12150079
1 0.807 0.280 17 39869164 intron variant G/A snv 0.24 0.700 1.000 2 2010 2011
dbSNP: rs13314993
rs13314993
5 0.882 0.200 3 32973977 regulatory region variant G/C;T snv 0.700 1.000 2 2011 2011
dbSNP: rs13431828
rs13431828
2 0.925 0.160 2 102338193 5 prime UTR variant C/T snv 0.18 0.700 1.000 2 2010 2011
dbSNP: rs1464510
rs1464510
LPP
7 0.807 0.280 3 188394766 intron variant C/A;T snv 0.700 1.000 2 2011 2011
dbSNP: rs1736135
rs1736135
4 0.851 0.160 21 15432901 intron variant T/C snv 0.33 0.700 1.000 2 2011 2011
dbSNP: rs1810132
rs1810132
1 1.000 0.080 17 39709752 intron variant C/T snv 0.64 0.700 1.000 2 2010 2011
dbSNP: rs2271308
rs2271308
1 1.000 0.080 17 39661229 non coding transcript exon variant T/C snv 0.61 0.700 1.000 2 2010 2011
dbSNP: rs2548659
rs2548659
1 1.000 0.080 5 60088059 intron variant A/G snv 0.28 0.700 1.000 2 2009 2010
dbSNP: rs802734
rs802734
5 0.827 0.280 6 127957653 intergenic variant A/G;T snv 0.700 1.000 2 2011 2011
dbSNP: rs983280
rs983280
1 1.000 0.080 5 60149310 intron variant C/T snv 0.68 0.700 1.000 2 2009 2010
dbSNP: rs10045431
rs10045431
3 0.851 0.240 5 159387525 intron variant A/C snv 0.78 0.700 1.000 1 2011 2011
dbSNP: rs1007654
rs1007654
1 1.000 0.080 17 39955101 intron variant A/G snv 0.69 0.700 1.000 1 2010 2010
dbSNP: rs10173081
rs10173081
2 1.000 0.080 2 102340888 intron variant C/T snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs10189629
rs10189629
2 1.000 0.080 2 102263004 regulatory region variant C/A snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs10204137
rs10204137
1 0.925 0.160 2 102351752 missense variant A/G;T snv 0.34 0.700 1.000 1 2010 2010
dbSNP: rs10206753
rs10206753
2 1.000 0.080 2 102351902 missense variant T/C;G snv 0.34; 4.0E-06 0.700 1.000 1 2010 2010
dbSNP: rs10211025
rs10211025
1 1.000 0.080 2 41801493 intergenic variant A/G snv 0.12 0.700 1.000 1 2014 2014
dbSNP: rs1043828
rs1043828
2 1.000 0.080 5 111128310 3 prime UTR variant T/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs10445308
rs10445308
3 0.851 0.240 17 39781794 intron variant C/T snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs1054609
rs1054609
2 0.925 0.160 17 39877024 3 prime UTR variant A/C snv 0.40 0.700 1.000 1 2011 2011
dbSNP: rs1061477
rs1061477
1 1.000 0.080 19 50856840 intron variant T/C snv 0.42 0.700 1.000 1 2012 2012
dbSNP: rs10758669
rs10758669
5 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs10800812
rs10800812
1 1.000 0.080 1 202086810 intergenic variant A/G snv 0.77 0.700 1.000 1 2000 2000