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: rs337705
rs337705
1 1.000 0.080 5 114401365 intron variant T/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs337711
rs337711
1 1.000 0.080 5 114412874 intron variant C/T snv 0.48 0.700 1.000 1 2017 2017
dbSNP: rs716845
rs716845
1 1.000 0.080 5 114400719 intron variant G/A snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs13184658
rs13184658
1 1.000 0.080 5 114394710 intron variant G/A snv 0.27 0.010 1.000 1 2016 2016