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: rs13191343
rs13191343
1 1.000 0.080 6 31273332 intron variant C/G;T snv 0.13 0.800 1.000 1 2010 2010
dbSNP: rs115429782
rs115429782
1 1.000 0.080 6 31297975 intron variant T/C snv 0.700 1.000 1 2019 2019
dbSNP: rs12191877
rs12191877
7 0.851 0.120 6 31285148 intron variant C/T snv 0.12 0.700 1.000 1 2015 2015
dbSNP: rs12189871
rs12189871
2 0.925 0.080 6 31284147 intron variant C/T snv 8.6E-02 0.010 1.000 1 2015 2015