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: rs3814231
rs3814231
1 1.000 0.040 10 113721259 intron variant C/T snv 0.23 0.800 1.000 1 2012 2012
dbSNP: rs12771452
rs12771452
1 1.000 0.040 10 113728572 intron variant G/A snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs4353229
rs4353229
6 0.807 0.160 10 113729830 3 prime UTR variant T/C snv 0.23 0.010 1.000 1 2015 2015