Source: ALL
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: rs12474609
rs12474609
LRP1B
1 2 140963573 intron variant A/T snv 0.18 0.700 1.000 1 2010 2010
dbSNP: rs294588
rs294588 		1 5 163571509 regulatory region variant T/C snv 0.70 0.700 1.000 1 2013 2013
dbSNP: rs6925255
rs6925255 		1 6 79756407 regulatory region variant A/C;G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs9918668
rs9918668
LOC107986820
1 7 94062432 intron variant G/A snv 0.47 0.700 1.000 1 2013 2013