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: rs2236668
rs2236668
1 1.000 0.120 21 44230126 intron variant T/A;C;G snv 7.1E-05; 0.40; 0.26; 4.1E-05 0.800 1.000 1 2014 2019
dbSNP: rs397897657
rs397897657
1 1.000 0.120 21 44230126 intron variant -/G delins 1.7E-04 0.700 1.000 1 2014 2014
dbSNP: rs56323213
rs56323213
1 1.000 0.120 21 44230126 intron variant -/G delins 0.700 1.000 1 2014 2014