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: rs509345
rs509345
1 1 150303594 intron variant A/G snv 0.58 0.700 1.000 1 2019 2019
dbSNP: rs543179
rs543179
1 1 150302182 intron variant G/A snv 0.46 0.700 1.000 1 2019 2019