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: rs582537
rs582537
1 1.000 0.080 3 159992311 intron variant A/C;G snv 0.800 1.000 2 2012 2017
dbSNP: rs582054
rs582054
5 0.882 0.160 3 159992214 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs647801
rs647801
1 1.000 0.080 3 159989732 intron variant A/G snv 0.58 0.700 1.000 1 2012 2012