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: rs2368564
rs2368564
REN
1 1.000 0.040 1 204155737 intron variant C/G;T snv 0.010 1.000 1 2018 2018
dbSNP: rs6682082
rs6682082
REN
1 1.000 0.040 1 204167813 intron variant C/T snv 0.18 0.010 1.000 1 2015 2015
dbSNP: rs777208537
rs777208537
REN
2 1.000 0.040 1 204156313 synonymous variant A/G snv 4.0E-06 0.010 1.000 1 2001 2001