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: rs174547
rs174547
33 0.742 0.240 11 61803311 intron variant T/C snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs174556
rs174556
7 0.925 0.160 11 61813163 intron variant C/T snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs968567
rs968567
7 0.851 0.240 11 61828092 intron variant C/T snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs174548
rs174548
17 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 0.700 1.000 1 2008 2008
dbSNP: rs174550
rs174550
13 0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 0.700 1.000 1 2011 2011