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: rs5756931
rs5756931
1 22 38150026 non coding transcript exon variant T/A;C snv 0.800 1.000 3 2010 2018
dbSNP: rs2277844
rs2277844
2 22 38181508 intron variant G/A snv 0.53 0.800 1.000 2 2012 2016
dbSNP: rs133027
rs133027
2 22 38179492 intron variant T/- delins 0.46 0.700 1.000 1 2018 2018
dbSNP: rs133029
rs133029
1 22 38180308 intron variant C/T snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs3761445
rs3761445
2 22 38199404 intron variant G/A snv 0.52 0.700 1.000 1 2017 2017
dbSNP: rs4820323
rs4820323
4 22 38203760 non coding transcript exon variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs55951234
rs55951234
2 22 38205423 5 prime UTR variant -/CTC delins 0.700 1.000 1 2018 2018