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: rs4862423
rs4862423
4 0.882 0.080 4 184805394 intron variant C/T snv 0.37 0.010 1.000 1 2016 2016
dbSNP: rs735949
rs735949
3 0.925 0.080 4 184795078 intron variant T/C snv 0.10 0.010 1.000 1 2016 2016