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: rs17158898
rs17158898
1 10 45725002 intron variant T/A snv 4.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs17159090
rs17159090
1 10 45712353 intron variant C/T snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs17159119
rs17159119
1 10 45720318 intron variant C/T snv 8.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs17696112
rs17696112
1 10 45715303 intron variant C/T snv 2.5E-02 0.700 1.000 1 2012 2012