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: rs2163188
rs2163188
1 10 63554951 intron variant G/A;C snv 0.700 1.000 2 2017 2018
dbSNP: rs10761785
rs10761785
3 10 63559006 intron variant G/T snv 0.51 0.700 1.000 1 2019 2019