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: rs2814778
rs2814778
24 0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 0.800 1.000 6 2011 2019
dbSNP: rs34599082
rs34599082
8 1 159205704 missense variant C/T snv 1.1E-02 9.9E-03 0.700 1.000 1 2016 2016
dbSNP: rs7550207
rs7550207
5 1 159205095 intron variant T/C snv 0.19 0.700 1.000 1 2016 2016