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: rs7190997
rs7190997
2 1.000 0.120 16 31356857 intron variant T/C snv 0.52 0.710 1.000 2 2015 2019
dbSNP: rs11574637
rs11574637
3 0.882 0.200 16 31357553 missense variant T/C snv 0.21 0.700 1.000 1 2014 2014
dbSNP: rs11150619
rs11150619
2 0.925 0.160 16 31365528 intron variant T/C snv 0.29 0.010 1.000 1 2019 2019