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: rs2030323
rs2030323
6 0.925 0.080 11 27706992 intron variant A/C snv 0.83 0.800 1.000 1 2013 2013
dbSNP: rs10835211
rs10835211
3 1.000 0.080 11 27679818 intron variant G/A snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs6265
rs6265
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.100 0.905 21 2005 2019
dbSNP: rs759834365
rs759834365
237 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 0.100 0.923 13 2005 2019
dbSNP: rs746682028
rs746682028
36 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 0.030 1.000 3 2007 2017
dbSNP: rs10767664
rs10767664
16 0.752 0.400 11 27704439 intron variant T/A snv 0.83 0.020 1.000 2 2017 2017
dbSNP: rs12291063
rs12291063
1 1.000 0.080 11 27672554 intron variant T/C snv 0.12 0.010 1.000 1 2015 2015