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: rs4846914
rs4846914
4 0.925 0.080 1 230159944 intron variant G/A snv 0.45 0.800 1.000 5 2008 2019
dbSNP: rs2144300
rs2144300
4 0.882 0.040 1 230159169 intron variant C/T snv 0.44 0.800 1.000 2 2008 2018
dbSNP: rs10489615
rs10489615
2 1 230169242 intron variant A/C;G snv 0.800 1.000 1 2010 2010
dbSNP: rs4846918
rs4846918
3 1 230164840 intron variant C/G;T snv 0.700 1.000 2 2012 2012
dbSNP: rs17315646
rs17315646
3 1 230159560 intron variant C/A;G snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs2281719
rs2281719
3 1.000 0.040 1 230161913 intron variant C/T snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs2296065
rs2296065
3 1 230166030 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs4846908
rs4846908
2 1 230149309 intron variant G/A snv 0.43 0.700 1.000 1 2012 2012
dbSNP: rs609526
rs609526
2 1 230173160 intron variant T/A snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs611229
rs611229
2 1 230188321 intron variant T/G snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs611841
rs611841
3 1 230173735 intron variant C/A;G snv 0.700 1.000 1 2012 2012