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: rs7914926
rs7914926
1 10 79170941 intron variant A/G snv 0.41 0.700 1.000 1 2017 2017
dbSNP: rs7916441
rs7916441
3 10 79165820 intron variant G/C snv 0.39 0.700 1.000 1 2019 2019