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: rs10941235
rs10941235
2 0.925 0.080 5 35185478 intron variant C/T snv 0.32 0.010 1.000 1 2011 2011
dbSNP: rs13436213
rs13436213
2 0.925 0.080 5 35185724 intron variant C/T snv 0.31 0.010 1.000 1 2011 2011
dbSNP: rs249537
rs249537
2 0.925 0.080 5 35089198 intron variant G/A snv 0.27 0.010 1.000 1 2011 2011
dbSNP: rs7718468
rs7718468
2 0.925 0.080 5 35200934 intron variant A/G snv 0.27 0.010 1.000 1 2011 2011