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: rs11218343
rs11218343
1 0.925 0.080 11 121564878 intron variant T/A;C snv 0.830 1.000 2 2013 2019
dbSNP: rs3781834
rs3781834
1 1.000 0.080 11 121575231 intron variant A/G snv 2.5E-02 0.700 1.000 1 2013 2013