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: rs3824999
rs3824999
9 0.790 0.080 11 74634505 intron variant T/G snv 0.40 0.700 1.000 4 2012 2019
dbSNP: rs57796856
rs57796856
9 0.790 0.080 11 74627310 intron variant A/T snv 0.39 0.700 1.000 1 2019 2019
dbSNP: rs7121958
rs7121958
10 0.776 0.080 11 74568967 intron variant T/A;G snv 0.700 1.000 1 2019 2019