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: rs2243868
rs2243868
2 0.925 0.160 6 31293499 intron variant A/G snv 0.66 0.700 1.000 2 2007 2011
dbSNP: rs2524089
rs2524089
3 0.925 0.160 6 31298745 intron variant G/T snv 0.65 0.700 1.000 2 2007 2011
dbSNP: rs1960278
rs1960278
2 0.925 0.160 6 31302097 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs2246954
rs2246954
2 0.925 0.160 6 31297485 intron variant A/G snv 0.60 0.700 1.000 1 2011 2011
dbSNP: rs2524066
rs2524066
2 0.925 0.160 6 31301377 intron variant T/C snv 0.65 0.700 1.000 1 2011 2011
dbSNP: rs2524095
rs2524095
2 0.925 0.160 6 31298340 intron variant A/C snv 0.65 0.700 1.000 1 2011 2011
dbSNP: rs2853918
rs2853918
2 0.925 0.160 6 31300843 intron variant C/T snv 0.65 0.700 1.000 1 2011 2011
dbSNP: rs3873379
rs3873379
5 0.925 0.120 6 31294392 intron variant T/C snv 0.35 0.700 1.000 1 2007 2007
dbSNP: rs9366778
rs9366778
6 0.925 0.120 6 31301396 intron variant G/A snv 0.47 0.700 1.000 1 2007 2007