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: rs3780181
rs3780181
4 1.000 0.320 9 2640759 intron variant A/G snv 0.11 0.800 1.000 3 2013 2018
dbSNP: rs34548991
rs34548991
2 9 2628957 intron variant C/T snv 1.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs34998951
rs34998951
3 9 2634144 intron variant A/G snv 6.7E-03 0.700 1.000 1 2012 2012
dbSNP: rs35466361
rs35466361
2 9 2641107 intron variant T/A snv 2.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs35486699
rs35486699
2 9 2640605 intron variant C/T snv 2.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs7024888
rs7024888
2 9 2636992 intron variant T/C snv 9.1E-02 0.700 1.000 1 2012 2012