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: rs11640716
rs11640716
1 1.000 0.040 16 50631178 intron variant T/A;G snv 0.700 1.000 1 2007 2007
dbSNP: rs12913
rs12913
1 1.000 0.040 16 50634515 3 prime UTR variant T/C snv 0.61 0.700 1.000 1 2007 2007
dbSNP: rs12924696
rs12924696
1 1.000 0.040 16 50637810 3 prime UTR variant G/A;C snv 0.700 1.000 1 2007 2007
dbSNP: rs1558663
rs1558663
1 1.000 0.040 16 50628933 intron variant G/A snv 0.57 0.700 1.000 1 2007 2007
dbSNP: rs4785220
rs4785220
1 1.000 0.040 16 50593467 intron variant T/C snv 0.77 0.700 1.000 1 2007 2007
dbSNP: rs7198686
rs7198686
1 1.000 0.040 16 50632655 intron variant T/A;C snv 0.700 1.000 1 2007 2007
dbSNP: rs745230
rs745230
1 1.000 0.040 16 50636271 3 prime UTR variant G/A;C;T snv 0.700 1.000 1 2007 2007
dbSNP: rs8046845
rs8046845
1 1.000 0.040 16 50626853 intron variant G/A;C snv 0.700 1.000 1 2007 2007
dbSNP: rs9926095
rs9926095
1 1.000 0.040 16 50645404 3 prime UTR variant A/C;T snv 0.700 1.000 1 2007 2007