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: rs4237036
rs4237036
1 8 60788498 intron variant C/T snv 0.52 0.700 1.000 1 2018 2018
dbSNP: rs7846314
rs7846314
5 8 60738272 intron variant A/T snv 0.27 0.700 1.000 1 2016 2016