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: rs3786897
rs3786897
5 1.000 0.080 19 33402102 intron variant A/G snv 0.45 0.700 1.000 3 2015 2019
dbSNP: rs3786898
rs3786898
1 19 33403137 intron variant G/A snv 0.44 0.700 1.000 1 2019 2019