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: rs7846314
rs7846314
5 8 60738272 intron variant A/T snv 0.27 0.700 1.000 2 2016 2019
dbSNP: rs10094382
rs10094382
1 8 60860726 intron variant C/T snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs13280978
rs13280978
1 8 60791496 intron variant C/T snv 0.52 0.700 1.000 1 2018 2018