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: rs267607619
rs267607619
3 0.882 0.160 1 156130666 missense variant G/C snv 0.010 1.000 1 2015 2015
dbSNP: rs267607639
rs267607639
3 0.882 0.200 1 156136939 missense variant T/C snv 0.010 1.000 1 2003 2003
dbSNP: rs57077886
rs57077886
9 0.776 0.240 1 156114947 missense variant C/T snv 0.010 1.000 1 2018 2018
dbSNP: rs58932704
rs58932704
8 0.776 0.200 1 156136413 missense variant C/T snv 0.010 1.000 1 2003 2003