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: rs17643262
rs17643262
1 1.000 0.080 19 45128558 intron variant G/A snv 9.9E-02 0.800 1.000 2 2011 2018
dbSNP: rs346763
rs346763
1 1.000 0.080 19 45226017 intron variant G/A snv 0.10 0.800 1.000 1 2014 2018
dbSNP: rs10416371
rs10416371
1 1.000 0.080 19 45156878 intron variant A/C;T snv 0.700 1.000 2 2011 2012
dbSNP: rs10415983
rs10415983
1 1.000 0.080 19 45208340 intron variant C/T snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs10422797
rs10422797
1 1.000 0.080 19 45222848 intron variant T/C snv 8.9E-02 0.700 1.000 1 2011 2011
dbSNP: rs1048699
rs1048699
2 1.000 0.080 19 45147128 3 prime UTR variant C/T snv 9.0E-02 0.700 1.000 1 2011 2011
dbSNP: rs1114831
rs1114831
1 1.000 0.080 19 45133061 intron variant C/A snv 9.5E-02 0.700 1.000 1 2011 2011
dbSNP: rs1114832
rs1114832
2 1.000 0.080 19 45132943 intron variant C/T snv 9.2E-02 0.700 1.000 1 2011 2011