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: rs9788269
rs9788269
1 12 93801114 intron variant A/G snv 0.23 0.700 1.000 2 2019 2019
dbSNP: rs11107184
rs11107184
1 12 93790306 intron variant C/T snv 0.31 0.700 1.000 1 2018 2018