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: rs1039002
rs1039002
5 0.846 0.071 6 165741969 intron variant G/A,T snp 5.7E-02 0.010 1.000 1 2012 2012
dbSNP: rs2023239
rs2023239
8 0.784 0.143 6 88150763 intron variant T/C snp 0.19 0.010 1.000 1 2008 2008
dbSNP: rs3278
rs3278
1 1.000 0.071 3 27433860 intron variant G/A snp 0.12 0.010 1.000 1 2007 2007
dbSNP: rs135745
rs135745
5 0.878 0.071 22 38287631 intergenic variant G/C snp 0.47 0.010 < 0.001 1 2008 2008
dbSNP: rs6265
rs6265
171 0.463 0.679 11 27658369 missense variant C/T snp 0.19 0.15 0.020 1.000 2 2006 2009
dbSNP: rs759834365
rs759834365
157 0.471 0.679 11 27658456 missense variant C/T snp 1.2E-05 0.020 1.000 2 2006 2009
dbSNP: rs2465811
rs2465811
1 1.000 0.071 12 70596274 missense variant T/A,C snp 0.27; 3.2E-05 0.30 0.010 1.000 1 2008 2008
dbSNP: rs324420
rs324420
36 0.657 0.321 1 46405089 missense variant C/A snp 0.24 0.28 0.010 1.000 1 2008 2008
dbSNP: rs746682028
rs746682028
29 0.652 0.429 11 27658414 missense variant C/A,T snp 4.0E-06; 4.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs6296
rs6296
12 0.769 0.071 6 77462543 synonymous variant C/G snp 0.31 0.27 0.010 1.000 1 2003 2003