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: rs17028615
rs17028615
4 1.000 0.080 4 99150767 intron variant A/C;G snv 0.700 1.000 1 2014 2014
dbSNP: rs5860563
rs5860563
3 1.000 0.080 4 99126006 intron variant -/A delins 0.700 1.000 1 2019 2019
dbSNP: rs1042364
rs1042364
1 1.000 0.080 4 99124423 stop gained T/A;C snv 0.78 0.020 1.000 2 2011 2016
dbSNP: rs1800759
rs1800759
4 0.925 0.120 4 99144358 intron variant T/G snv 0.49 0.020 1.000 2 2006 2011
dbSNP: rs3762894
rs3762894
2 1.000 0.080 4 99144933 intron variant T/C snv 0.19 0.020 1.000 2 2011 2011
dbSNP: rs10009145
rs10009145
1 1.000 0.080 4 99126778 intron variant G/A snv 0.39 0.34 0.010 1.000 1 2012 2012
dbSNP: rs1126671
rs1126671
5 0.851 0.120 4 99127263 missense variant T/C snv 0.76 0.75 0.010 1.000 1 2005 2005
dbSNP: rs7689753
rs7689753
1 1.000 0.080 4 99134424 intron variant A/G snv 0.21 0.010 1.000 1 2012 2012