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: rs10738445
rs10738445
1 1.000 0.160 9 16680140 intron variant A/C;T snv 0.010 1.000 1 2017 2017
dbSNP: rs3904778
rs3904778
3 0.882 0.200 9 16681995 intron variant C/G snv 0.62 0.010 1.000 1 2018 2018