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: rs45546039
rs45546039
10 0.769 0.107 3 38613781 missense variant C/A,T snp 4.1E-06 0.710 1.000 9 2010 2013
dbSNP: rs199473161
rs199473161
2 1.000 0.071 3 38586038 missense variant G/A snp 0.700 6 2005 2015
dbSNP: rs137854607
rs137854607
9 0.801 0.107 3 38554309 missense variant C/G,T snp 0.700 3 2005 2012
dbSNP: rs137854618
rs137854618
13 0.734 0.107 3 38566426 missense variant C/A,T snp 8.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs199473153
rs199473153
6 0.821 0.107 3 38597737 missense variant C/T snp 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs41310765
rs41310765
3 1.000 0.071 3 38575424 missense variant G/A snp 1.4E-04 1.9E-04 0.010 1.000 1 2009 2009