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: rs131746
rs131746
1 22 50587166 intron variant C/G snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs131748
rs131748
1 22 50586408 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs131749
rs131749
1 22 50586195 intron variant T/C snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs131750
rs131750
1 22 50585879 non coding transcript exon variant T/C snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs140513
rs140513
1 22 50589826 intron variant C/G;T snv 0.700 1.000 1 2012 2012