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: rs7428496
rs7428496
1 3 142601690 intron variant A/T snv 0.66 0.700 1.000 1 2016 2016
dbSNP: rs7615316
rs7615316
3 3 142637084 intron variant G/A snv 0.61 0.700 1.000 1 2017 2017