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: rs10854167
rs10854167
1 20 62901687 intron variant G/C snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs13040088
rs13040088
1 20 62917850 intron variant A/G snv 0.19 0.700 1.000 1 2015 2015