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: rs1060848
rs1060848
1 10 45616502 synonymous variant A/G snv 3.1E-02 3.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs17157944
rs17157944
1 10 45652818 intron variant A/G snv 6.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs17157945
rs17157945
1 10 45652853 intron variant T/A snv 6.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs17696005
rs17696005
1 10 45653302 intron variant C/T snv 2.5E-02 0.700 1.000 1 2012 2012