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: rs4434553
rs4434553
5 1.000 0.040 7 100642568 intron variant A/G snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs4729597
rs4729597
2 7 100624226 intron variant C/T snv 0.69 0.700 1.000 1 2019 2019
dbSNP: rs62482241
rs62482241
2 7 100637885 intron variant G/A snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs7385804
rs7385804
14 0.851 0.120 7 100638347 intron variant C/A snv 0.65 0.700 1.000 1 2016 2016