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: rs11783469
rs11783469
1 8 23543882 intron variant C/T snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs12549025
rs12549025
1 8 23542024 intron variant A/G snv 0.14 0.700 1.000 1 2016 2016