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 2016 2016
dbSNP: rs381815
rs381815
6 1.000 0.040 11 16880721 intron variant C/A;T snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs7940807
rs7940807
2 11 16892459 intron variant G/T snv 0.21 0.700 1.000 1 2018 2018