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: rs259919
rs259919
6 0.882 0.080 6 30057726 intron variant G/A snv 0.25 0.800 1.000 1 2009 2009
dbSNP: rs7758512
rs7758512
4 1.000 6 30002812 intron variant T/G snv 0.17 0.800 1.000 1 2009 2009
dbSNP: rs3869068
rs3869068
5 0.925 6 30036275 intron variant C/T snv 0.17 0.700 1.000 1 2009 2009
dbSNP: rs9261129
rs9261129
4 1.000 6 30011802 intron variant T/C snv 0.17 0.700 1.000 1 2009 2009
dbSNP: rs9261174
rs9261174
4 1.000 6 30029078 intron variant T/C snv 0.17 0.700 1.000 1 2009 2009