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: rs10850185
rs10850185
1 12 113627607 intron variant C/A snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs16942944
rs16942944
1 12 113628504 intron variant G/A snv 0.29 0.700 1.000 1 2019 2019