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: rs10410606
rs10410606
1 19 40603069 intron variant A/C snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs34093919
rs34093919
3 19 40611394 missense variant G/A snv 7.7E-03 7.5E-03 0.700 1.000 1 2019 2019