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: rs41305481
rs41305481
1 9 99005103 intron variant A/G snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs7861925
rs7861925
1 9 99023316 intron variant G/A;T snv 2.8E-05; 0.14 0.700 1.000 1 2018 2018