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: rs16951001
rs16951001
1 15 67561903 intron variant G/T snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs16951275
rs16951275
2 15 67784830 intron variant T/C snv 0.30 0.700 1.000 1 2017 2017