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: rs6265
rs6265
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.700 1.000 3 2009 2013
dbSNP: rs11030104
rs11030104
12 0.790 0.240 11 27662970 intron variant A/G snv 0.16 0.700 1.000 1 2014 2014
dbSNP: rs1401635
rs1401635
4 0.925 0.040 11 27672444 intron variant C/G snv 0.73 0.700 1.000 1 2013 2013
dbSNP: rs925946
rs925946
9 0.882 0.120 11 27645655 intron variant T/G snv 0.72 0.700 1.000 1 2009 2009