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: rs11209026
rs11209026
5 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.900 0.944 8 2006 2020
dbSNP: rs2076756
rs2076756
2 0.882 0.040 16 50722970 intron variant A/G snv 0.17 0.830 1.000 6 2007 2019
dbSNP: rs11465804
rs11465804
3 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 0.800 1.000 4 2006 2010
dbSNP: rs199883290
rs199883290
2 0.925 0.120 16 50729867 missense variant G/A;C snv 4.0E-06; 1.5E-02 7.0E-06 0.700 1.000 4 2007 2012
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: rs2542151
rs2542151
6 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 0.880 1.000 4 2007 2016
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: rs1893217
rs1893217
8 0.742 0.440 18 12809341 intron variant A/G snv 0.12 0.850 1.000 3 2008 2016
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: rs212388
rs212388
4 0.827 0.240 6 159069404 intron variant C/G;T snv 0.810 1.000 3 2010 2017
dbSNP: rs3764147
rs3764147
4 0.807 0.280 13 43883789 missense variant A/G snv 0.28 0.27 0.810 1.000 3 2008 2017
dbSNP: rs6478109
rs6478109
2 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 0.830 1.000 3 2005 2016
dbSNP: rs9858542
rs9858542
BSN
2 0.925 0.040 3 49664550 synonymous variant G/A snv 0.26 0.27 0.810 1.000 3 2007 2010
dbSNP: rs10045431
rs10045431
3 0.851 0.240 5 159387525 intron variant A/C snv 0.78 0.810 1.000 2 2008 2014
dbSNP: rs10188217
rs10188217
1 0.925 0.080 2 60990407 intron variant T/A;C snv 0.800 1.000 2 2008 2011
dbSNP: rs10758669
rs10758669
5 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 0.850 1.000 2 2008 2016
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: rs10889677
rs10889677
2 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 0.850 1.000 2 2006 2020
dbSNP: rs11742570
rs11742570
2 0.925 0.040 5 40410482 upstream gene variant T/C;G snv 0.800 1.000 2 2010 2017
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: rs13003464
rs13003464
7 0.827 0.200 2 60959694 intron variant A/G snv 0.50 0.800 1.000 2 2008 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: rs1456896
rs1456896
2 0.882 0.200 7 50264865 upstream gene variant C/T snv 0.67 0.800 1.000 2 2008 2017
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