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: rs2071746
rs2071746
18 0.708 0.320 22 35380679 intron variant A/T snv 0.49 0.010 1.000 1 2011 2011
dbSNP: rs2071749
rs2071749
2 0.925 0.120 22 35387420 intron variant A/G snv 0.64 0.010 1.000 1 2011 2011
dbSNP: rs9607267
rs9607267
1 1.000 0.040 22 35385214 intron variant T/C snv 0.27 0.010 1.000 1 2009 2009