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: rs12459350
rs12459350
3 0.925 0.200 19 2176587 intron variant A/G snv 0.46 0.700 1.000 2 2018 2019
dbSNP: rs11882273
rs11882273
1 19 2173837 intron variant T/C snv 0.46 0.700 1.000 1 2019 2019