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: rs5029939
rs5029939
19 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.010 1.000 1 2015 2015
dbSNP: rs77191406
rs77191406
12 0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 0.010 1.000 1 2016 2016