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: rs1049673
rs1049673
7 0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 0.010 1.000 1 2014 2014
dbSNP: rs1761667
rs1761667
12 0.752 0.320 7 80615623 intron variant G/A snv 0.49 0.010 1.000 1 2019 2019
dbSNP: rs2065666
rs2065666
1 1.000 0.040 7 80601491 intron variant G/A;C snv 0.010 1.000 1 2016 2016
dbSNP: rs771676129
rs771676129
7 0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs999947969
rs999947969
7 0.827 0.080 7 80671145 synonymous variant C/T snv 0.010 1.000 1 2007 2007