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: rs540385376
rs540385376
5 0.925 0.120 6 31117605 non coding transcript exon variant C/A snv 0.700 1.000 1 2010 2010
dbSNP: rs541134362
rs541134362
4 1.000 6 31118905 intron variant C/T snv 0.700 1.000 1 2010 2010
dbSNP: rs546583999
rs546583999
4 1.000 6 31118105 non coding transcript exon variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs553317370
rs553317370
4 1.000 6 31121348 intron variant A/G snv 0.700 1.000 1 2010 2010
dbSNP: rs555542204
rs555542204
4 1.000 6 31118625 non coding transcript exon variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs573422310
rs573422310
4 1.000 6 31121079 intron variant T/C snv 0.700 1.000 1 2010 2010
dbSNP: rs575513907
rs575513907
4 1.000 6 31117187 missense variant T/C snv 0.700 1.000 1 2010 2010