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: rs61755320
rs61755320
41 0.716 0.520 16 89546737 missense variant C/T snv 2.9E-03 3.5E-03 0.720 1.000 15 2006 2018
dbSNP: rs760818649
rs760818649
2 0.925 0.080 16 89531963 frameshift variant C/-;CC delins 0.700 1.000 6 2008 2017
dbSNP: rs562890289
rs562890289
1 1.000 0.080 16 89544770 stop gained C/T snv 1.2E-05 3.5E-05 0.700 1.000 1 2017 2017
dbSNP: rs768136171
rs768136171
2 0.925 0.080 16 89529489 frameshift variant TG/- delins 8.0E-06 2.1E-05 0.700 1.000 1 1998 1998
dbSNP: rs768823392
rs768823392
10 0.827 0.120 16 89546657 coding sequence variant GGCGGGAGA/- delins 2.6E-04 4.2E-04 0.700 1.000 1 2017 2017
dbSNP: rs912983346
rs912983346
1 1.000 0.080 16 89513037 missense variant G/C snv 4.4E-06 7.0E-06 0.700 1.000 1 2017 2017