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: rs3771180
rs3771180
2 1.000 0.080 2 102337157 5 prime UTR variant G/A;T snv 0.820 1.000 1 2011 2019
dbSNP: rs3771166
rs3771166
2 1.000 0.080 2 102369762 intron variant G/A;T snv 0.810 1.000 3 2010 2012
dbSNP: rs13408661
rs13408661
2 1.000 0.080 2 102338622 intron variant G/A snv 0.18 0.810 1.000 2 2011 2012
dbSNP: rs10197862
rs10197862
2 0.925 0.120 2 102350089 intron variant A/G snv 0.18 0.810 1.000 1 2011 2014
dbSNP: rs9807989
rs9807989
1 1.000 0.080 2 102354740 intron variant T/C;G snv 0.46 0.800 1.000 1 2012 2012
dbSNP: rs10192157
rs10192157
2 1.000 0.080 2 102351896 missense variant C/T snv 0.34 0.46 0.710 1.000 1 2010 2020
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: rs10173081
rs10173081
2 1.000 0.080 2 102340888 intron variant C/T snv 0.18 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: rs13408569
rs13408569
2 1.000 0.080 2 102338596 intron variant G/C snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs1362348
rs1362348
2 1.000 0.080 2 102368164 intron variant C/G snv 0.45 0.700 1.000 1 2011 2011
dbSNP: rs3755276
rs3755276
2 0.925 0.120 2 102361999 intron variant C/T snv 0.45 0.700 1.000 1 2011 2011