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: rs3782889
rs3782889
5 0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 0.700 1.000 2 2011 2013
dbSNP: rs11065774
rs11065774
1 1.000 0.040 12 110917522 intron variant G/A snv 4.7E-02 0.700 1.000 1 2011 2011
dbSNP: rs3825389
rs3825389
1 1.000 0.040 12 110912967 intron variant C/T snv 7.1E-02 0.700 1.000 1 2011 2011