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: rs61752717
rs61752717
72 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 0.020 1.000 2 2010 2013
dbSNP: rs224217
rs224217
2 0.925 0.040 16 3251757 intron variant G/A snv 0.44 0.010 1.000 1 2009 2009
dbSNP: rs224222
rs224222
15 0.724 0.440 16 3254463 missense variant C/T snv 0.24 0.21 0.010 1.000 1 2009 2009
dbSNP: rs224223
rs224223
1 1.000 0.040 16 3254573 synonymous variant G/T snv 0.43 0.48 0.010 1.000 1 2009 2009
dbSNP: rs224224
rs224224
2 0.925 0.080 16 3254654 synonymous variant T/A;C snv 1.7E-04; 0.44 0.010 1.000 1 2009 2009
dbSNP: rs224225
rs224225
1 1.000 0.040 16 3254762 synonymous variant A/G snv 0.44 0.48 0.010 1.000 1 2009 2009