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: rs59918340
rs59918340
1 8 141222157 intron variant A/G snv 0.51 0.700 1.000 1 2016 2016
dbSNP: rs753778
rs753778
1 8 141218810 missense variant G/A snv 0.35 0.33 0.700 1.000 1 2016 2016