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: rs140876547
rs140876547
1 11 45962517 intron variant G/A snv 3.2E-03 0.700 1.000 1 2019 2019
dbSNP: rs146033545
rs146033545
1 11 46072184 intron variant T/A;G snv 0.700 1.000 1 2019 2019