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: rs548181
rs548181
5 0.851 0.040 11 125591814 5 prime UTR variant A/G snv 0.83 0.810 1.000 3 2011 2015
dbSNP: rs11220082
rs11220082
1 1.000 0.040 11 125454069 intron variant C/T snv 0.46 0.800 1.000 2 2011 2012
dbSNP: rs597570
rs597570
1 1.000 0.040 11 125481576 missense variant A/T snv 0.15 0.19 0.020 1.000 2 2004 2007
dbSNP: rs559668
rs559668
1 1.000 0.040 11 125487880 intron variant C/T snv 0.21 0.010 1.000 1 2007 2007