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: rs10982456
rs10982456
1 9 114928478 intron variant T/C snv 0.57 0.700 1.000 1 2019 2019
dbSNP: rs3181348
rs3181348
2 9 114931904 intron variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs726657
rs726657
6 0.827 0.120 9 114934056 intron variant C/T snv 0.50 0.700 1.000 1 2016 2016