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: rs4766587
rs4766587
1 1.000 0.040 12 109247525 intron variant G/A snv 0.23 0.010 1.000 1 2010 2010
dbSNP: rs6606697
rs6606697
1 1.000 0.040 12 109173915 intron variant A/G snv 0.48 0.010 1.000 1 2010 2010