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: rs243866
rs243866
8 0.827 0.120 16 55477625 intron variant G/A snv 0.19 0.010 1.000 1 2019 2019
dbSNP: rs243865
rs243865
48 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.020 1.000 2 2018 2019
dbSNP: rs14070
rs14070
1 16 55502815 synonymous variant C/T snv 0.40 0.37 0.010 1.000 1 2019 2019
dbSNP: rs7201
rs7201
4 0.925 0.160 16 55505702 3 prime UTR variant A/C snv 0.37 0.010 1.000 1 2019 2019