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: rs9511952
rs9511952
1 1.000 0.040 13 25851530 intron variant C/T snv 0.13 0.700 1.000 1 2012 2012
dbSNP: rs9511955
rs9511955
1 1.000 0.040 13 25851915 intron variant T/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs9511957
rs9511957
1 1.000 0.040 13 25852663 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs9511958
rs9511958
1 1.000 0.040 13 25853625 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs9581465
rs9581465
1 1.000 0.040 13 25848944 intron variant A/C snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs9581467
rs9581467
1 1.000 0.040 13 25850231 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012