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: rs10758658
rs10758658
4 9 4856877 intron variant G/A snv 0.15 0.800 1.000 2 2009 2017
dbSNP: rs10758656
rs10758656
7 9 4852599 intron variant A/G snv 0.19 0.700 1.000 2 2017 2019
dbSNP: rs17803780
rs17803780
2 9 4849647 intron variant T/C snv 0.19 0.700 1.000 1 2016 2016
dbSNP: rs2236496
rs2236496
5 9 4844265 intron variant T/C snv 0.19 0.700 1.000 1 2010 2010
dbSNP: rs3824430
rs3824430
1 9 4847168 intron variant T/C snv 0.19 0.700 1.000 1 2018 2018