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: rs10900218
rs10900218
2 10 45465974 intron variant A/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs112297763
rs112297763
1 10 45573988 intron variant T/C snv 6.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs34285816
rs34285816
1 10 45481403 intron variant G/A snv 6.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs35993099
rs35993099
2 10 45511519 intron variant T/A snv 6.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs963029
rs963029
3 10 45467939 intron variant C/T snv 0.24 0.700 1.000 1 2009 2009