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: rs16891867
rs16891867
1 1.000 0.040 4 15395740 intron variant A/G snv 0.11 0.800 1.000 1 2011 2011
dbSNP: rs1861046
rs1861046
1 1.000 0.040 4 15396282 intron variant G/A snv 0.11 0.800 1.000 1 2011 2011