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: rs1480380
rs1480380
4 0.763 0.360 6 32945469 intron variant C/T snv 0.11 0.700 1.000 2 2007 2009
dbSNP: rs151719
rs151719
2 0.925 0.160 6 32936123 non coding transcript exon variant C/T snv 0.72 0.700 1.000 2 2007 2009
dbSNP: rs194682
rs194682
1 1.000 0.120 6 32946836 intron variant C/T snv 0.30 0.700 1.000 2 2007 2009
dbSNP: rs1042337
rs1042337
1 1.000 0.120 6 32937204 missense variant G/A snv 0.78 0.80 0.700 1.000 1 2009 2009
dbSNP: rs2395296
rs2395296
1 1.000 0.120 6 32944037 intron variant A/G snv 0.72 0.700 1.000 1 2009 2009