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: rs9349379
rs9349379
19 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.800 1.000 2 2011 2013
dbSNP: rs10807323
rs10807323
1 6 12794799 intron variant G/A snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs2026458
rs2026458
6 0.882 0.080 6 12825642 intron variant C/T snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs4711863
rs4711863
1 6 12915185 intron variant G/C snv 0.29 0.700 1.000 1 2011 2011