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 2010 2010
dbSNP: rs10499859
rs10499859
2 0.925 0.120 7 80629494 intron variant A/G snv 0.46 0.010 1.000 1 2012 2012
dbSNP: rs11760281
rs11760281
1 1.000 0.040 7 80475233 intron variant A/G snv 0.55 0.010 1.000 1 2012 2012
dbSNP: rs1194197
rs1194197
2 0.925 0.080 7 80546290 intron variant A/G snv 0.52 0.010 1.000 1 2012 2012
dbSNP: rs13246513
rs13246513
1 1.000 0.040 7 80677435 3 prime UTR variant C/G;T snv 0.36 0.010 1.000 1 2012 2012
dbSNP: rs1761667
rs1761667
12 0.752 0.320 7 80615623 intron variant G/A snv 0.49 0.010 1.000 1 2012 2012
dbSNP: rs3211931
rs3211931
3 0.925 0.080 7 80668857 intron variant C/T snv 0.38 0.010 1.000 1 2010 2010
dbSNP: rs75326924
rs75326924
4 0.882 0.120 7 80656687 missense variant C/T snv 1.1E-03 1.0E-04 0.010 1.000 1 2001 2001