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: rs10404046
rs10404046
1 19 16366444 intron variant G/C snv 0.63 0.700 1.000 1 2018 2018
dbSNP: rs10408945
rs10408945
1 19 16466180 intron variant G/T snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs10411936
rs10411936
3 1.000 0.080 19 16437564 intron variant A/G snv 0.63 0.700 1.000 1 2011 2011
dbSNP: rs7251806
rs7251806
1 19 16388758 intron variant C/A;G;T snv 0.700 1.000 1 2016 2016