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: rs11024074
rs11024074
5 0.925 0.040 11 16895672 intron variant T/C snv 0.29 0.700 1.000 1 2009 2009
dbSNP: rs177542
rs177542
1 11 16901107 intron variant G/A snv 0.47 0.700 1.000 1 2017 2017
dbSNP: rs381815
rs381815
6 1.000 0.040 11 16880721 intron variant C/A;T snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs416258
rs416258
3 11 16890089 intron variant G/C snv 0.29 0.700 1.000 1 2018 2018