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: rs12936231
rs12936231
3 0.925 0.160 17 39872867 intron variant C/G;T snv 0.720 1.000 1 2011 2019
dbSNP: rs11557467
rs11557467
4 0.851 0.200 17 39872381 missense variant G/T snv 0.45 0.45 0.710 1.000 1 2010 2011
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: 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: rs11078925
rs11078925
3 0.925 0.160 17 39868955 intron variant T/C snv 0.36 0.700 1.000 1 2011 2011
dbSNP: rs11557466
rs11557466
3 0.925 0.160 17 39868373 synonymous variant C/T snv 0.40 0.36 0.700 1.000 1 2011 2011
dbSNP: rs11870965
rs11870965
3 0.925 0.160 17 39873952 intron variant T/A snv 0.40 0.700 1.000 1 2011 2011