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: rs11668344
rs11668344
4 0.925 0.120 19 55322296 intron variant A/G snv 0.35 0.800 1.000 3 2012 2015
dbSNP: rs1172822
rs1172822
2 1.000 0.040 19 55308477 intron variant C/T snv 0.34 0.800 1.000 3 2009 2013
dbSNP: rs2384687
rs2384687
1 19 55319820 non coding transcript exon variant A/G snv 0.38 0.700 1.000 2 2009 2013
dbSNP: rs897798
rs897798
1 19 55322386 intron variant A/G snv 0.46 0.700 1.000 2 2009 2013
dbSNP: rs34962991
rs34962991
1 19 55315807 intron variant G/A snv 0.32 0.700 1.000 1 2019 2019