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: rs1464816
rs1464816
REN
2 1.000 0.120 1 204159726 intron variant T/C;G snv 0.010 1.000 1 2016 2016
dbSNP: rs371237692
rs371237692
REN
5 0.925 0.120 1 204159515 synonymous variant A/G snv 8.0E-06 3.5E-05 0.010 1.000 1 2012 2012