Source: ALL
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: rs5742904
rs5742904
APOB
22 0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 0.900 1.000 26 1989 2018
dbSNP: rs144467873
rs144467873
APOB
9 0.776 0.120 2 21006289 missense variant G/A snv 1.7E-04 6.3E-05 0.710 1.000 15 1989 2017
dbSNP: rs1215189537
rs1215189537
APOB
2 0.925 0.080 2 21007749 frameshift variant AAAGA/- delins 4.0E-06 0.700 1.000 2 2007 2012
dbSNP: rs368825685
rs368825685
APOB
2 0.925 0.080 2 21012365 stop gained A/C;G snv 4.0E-06; 1.2E-05 0.700 1.000 2 1993 2014
dbSNP: rs1558560212
rs1558560212
APOB
2 0.925 0.080 2 21004676 splice acceptor variant C/G snv 0.700 1.000 1 2010 2010
dbSNP: rs1558564161
rs1558564161
APOB
2 0.925 0.080 2 21010325 frameshift variant A/- delins 0.700 1.000 1 2012 2012
dbSNP: rs1553383017
rs1553383017
APOB
1 1.000 0.080 2 21006682 missense variant C/T snv 0.700 0
dbSNP: rs1553383473
rs1553383473
APOB
2 0.925 0.080 2 21009263 stop gained G/T snv 0.700 0
dbSNP: rs562574661
rs562574661
APOB
2 0.925 0.080 2 21001940 inframe deletion CTG/- delins 2.2E-04 0.700 0
dbSNP: rs730880052
rs730880052
APOB
1 1.000 0.080 2 21006681 missense variant G/T snv 0.700 0
dbSNP: rs766243954
rs766243954
APOB
2 0.925 0.080 2 21038086 stop gained C/A snv 7.0E-06 0.700 0
dbSNP: rs12713559
rs12713559
APOB
10 0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 0.010 1.000 1 1997 1997
dbSNP: rs200222843
rs200222843
APOB
4 0.851 0.120 2 21003286 missense variant G/A snv 4.0E-05 4.2E-05 0.010 1.000 1 1989 1989
dbSNP: rs757808215
rs757808215
LDLR
2 0.925 0.080 19 11106640 missense variant G/A;C;T snv 2.0E-05 0.010 1.000 1 1994 1994
dbSNP: rs779283285
rs779283285
APOB
1 1.000 0.080 2 21006393 missense variant A/G snv 1.6E-05 2.1E-05 0.010 1.000 1 2001 2001
dbSNP: rs929536329
rs929536329
LDLR
1 1.000 0.080 19 11105277 missense variant G/A snv 0.010 1.000 1 1994 1994