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: rs10224210
rs10224210
8 1.000 0.040 7 151716108 intron variant T/C snv 0.21 0.700 1.000 1 2017 2017
dbSNP: rs73728279
rs73728279
4 1.000 0.080 7 151714408 intron variant G/A;T snv 0.700 1.000 1 2019 2019