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: rs2241880
rs2241880
1 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 0.900 0.961 4 2007 2020
dbSNP: rs1343151
rs1343151
1 0.752 0.400 1 67253446 intron variant G/A snv 0.41 0.800 1.000 3 2006 2007
dbSNP: rs2066845
rs2066845
1 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 1.000 0.949 3 2001 2019
dbSNP: rs10188217
rs10188217
1 0.925 0.080 2 60990407 intron variant T/A;C snv 0.800 1.000 2 2008 2011
dbSNP: rs10883365
rs10883365
1 0.882 0.080 10 99528007 non coding transcript exon variant G/A snv 0.52 0.830 1.000 2 2007 2014
dbSNP: rs11805303
rs11805303
1 0.827 0.240 1 67209833 intron variant C/T snv 0.30 0.810 1.000 2 2007 2012
dbSNP: rs13361189
rs13361189
1 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 0.850 1.000 2 2007 2015
dbSNP: rs17221417
rs17221417
1 0.925 0.040 16 50705671 intron variant C/G snv 0.20 0.810 1.000 2 2007 2017
dbSNP: rs17234657
rs17234657
1 0.882 0.120 5 40401407 intergenic variant T/G snv 0.14 0.810 1.000 2 2007 2010
dbSNP: rs17309827
rs17309827
1 1.000 0.040 6 3433084 intron variant T/G snv 0.30 0.800 1.000 2 2008 2010
dbSNP: rs1736020
rs1736020
1 1.000 0.040 21 15440233 intron variant C/A snv 0.33 0.800 1.000 2 2008 2010
dbSNP: rs2024092
rs2024092
1 0.827 0.120 19 1124032 intron variant G/A snv 0.24 0.26 0.800 1.000 2 2008 2017
dbSNP: rs2066844
rs2066844
1 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 1.000 0.940 2 2001 2018
dbSNP: rs3792109
rs3792109
1 1.000 0.040 2 233275771 non coding transcript exon variant G/A snv 0.45 0.42 0.800 1.000 2 2010 2013
dbSNP: rs3810936
rs3810936
1 0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75 0.850 1.000 2 2005 2018
dbSNP: rs6651252
rs6651252
1 0.790 0.200 8 128554935 intron variant T/C snv 0.19 0.810 1.000 2 2010 2019
dbSNP: rs7702331
rs7702331
1 1.000 0.040 5 73255307 intron variant A/G snv 0.42 0.800 1.000 2 2010 2012
dbSNP: rs1000113
rs1000113
1 0.925 0.040 5 150860514 intron variant C/T snv 0.13 0.840 1.000 1 2007 2015
dbSNP: rs1002922
rs1002922
1 1.000 0.040 5 40386453 regulatory region variant T/C snv 0.29 0.700 1.000 1 2007 2007
dbSNP: rs1004819
rs1004819
1 0.776 0.360 1 67204530 intron variant G/A snv 0.30 0.860 1.000 1 2006 2019
dbSNP: rs10065637
rs10065637
1 1.000 0.040 5 56143024 intron variant C/T snv 0.15 0.800 1.000 1 2012 2012
dbSNP: rs10117785
rs10117785
1 1.000 0.040 9 114789323 3 prime UTR variant T/A snv 0.34 0.700 1.000 1 2005 2005
dbSNP: rs10181042
rs10181042
1 1.000 0.040 2 60997124 intron variant C/T snv 0.41 0.800 1.000 1 2010 2010
dbSNP: rs10210302
rs10210302
1 1.000 0.040 2 233250193 intron variant C/A;T snv 0.810 1.000 1 2007 2010
dbSNP: rs10484545
rs10484545
1 1.000 0.040 6 29266733 intron variant C/A;G snv 0.700 1.000 1 2007 2007