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: rs7775698
rs7775698
8 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 0.800 1.000 2 2009 2013
dbSNP: rs7776054
rs7776054
2 6 135097778 intron variant A/G snv 0.24 0.800 1.000 1 2009 2018
dbSNP: rs9399137
rs9399137
6 0.851 0.320 6 135097880 intron variant T/C snv 0.20 0.800 1.000 1 2013 2013
dbSNP: rs13220662
rs13220662
4 6 135074410 intron variant G/A snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs1547247
rs1547247
5 6 135069698 intron variant G/A snv 0.22 0.700 1.000 1 2012 2012