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: rs13210554
rs13210554
PLA2G7
1 1.000 0.080 6 46736602 upstream gene variant C/T snv 0.20 0.010 1.000 1 2009 2009
dbSNP: rs13301354
rs13301354
ABCA2 ; FUT7 ; C9orf139
1 1.000 0.080 9 137030185 3 prime UTR variant T/C snv 0.64 0.700 1.000 1 2011 2011
dbSNP: rs13306731
rs13306731
SOAT1
1 1.000 0.080 1 179351443 missense variant A/G snv 0.11 6.9E-02 0.010 1.000 1 2014 2014
dbSNP: rs1332329
rs1332329
LIPA
1 1.000 0.080 10 89243662 intron variant A/C snv 0.38 0.700 1.000 1 2015 2015
dbSNP: rs14309
rs14309
C17orf49 ; MIR497HG ; RNASEK-C17orf49
1 1.000 0.080 17 7015774 splice region variant T/C snv 0.80 0.76 0.010 1.000 1 2018 2018
dbSNP: rs1458301734
rs1458301734
APOE
1 1.000 0.080 19 44908687 missense variant G/A;T snv 5.9E-06 0.010 1.000 1 2004 2004
dbSNP: rs148267594
rs148267594
THBS2
1 1.000 0.080 6 169248872 missense variant C/A;T snv 6.2E-04 0.010 1.000 1 2019 2019
dbSNP: rs1548357
rs1548357
TXNRD2
1 1.000 0.080 22 19890839 intron variant T/C;G snv 0.010 1.000 1 2015 2015
dbSNP: rs1638021
rs1638021
PTPRN2
1 1.000 0.080 7 157645345 intron variant T/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs16980013
rs16980013
BHMG1
1 1.000 0.080 19 45764195 3 prime UTR variant G/T snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs17038082
rs17038082
NUP210
1 1.000 0.080 3 13358775 intron variant G/A snv 3.4E-02 0.700 1.000 1 2011 2011
dbSNP: rs17237890
rs17237890
CETP
1 1.000 0.080 16 56962246 5 prime UTR variant T/C snv 0.010 1.000 1 2017 2017
dbSNP: rs17381591
rs17381591
TRDMT1
1 1.000 0.080 10 17202049 non coding transcript exon variant T/C snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs17512204
rs17512204
CCDC93
1 1.000 0.080 2 117975255 missense variant G/A snv 5.6E-02 5.3E-02 0.010 1.000 1 2020 2020
dbSNP: rs17599586
rs17599586
ARG1 ; MED23
1 1.000 0.080 6 131583579 intron variant C/T snv 0.11 0.010 1.000 1 2007 2007
dbSNP: rs17708087
rs17708087 		1 1.000 0.080 17 40514261 upstream gene variant A/G snv 0.15 0.010 1.000 1 2016 2016
dbSNP: rs17828052
rs17828052
SORCS2
1 1.000 0.080 4 7484048 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs178293
rs178293
LZTR1
1 1.000 0.080 22 20995290 non coding transcript exon variant C/T snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs1794429
rs1794429
LRPAP1
1 1.000 0.080 4 3531339 intron variant C/T snv 0.68 0.700 1.000 1 2011 2011
dbSNP: rs1800774
rs1800774
CETP
1 1.000 0.080 16 56981633 intron variant C/A;T snv 4.0E-06; 0.32; 4.0E-06 0.010 < 0.001 1 2005 2005
dbSNP: rs1800791
rs1800791
FGB
1 1.000 0.080 4 154562157 upstream gene variant G/A snv 0.15 0.010 1.000 1 2006 2006
dbSNP: rs1878703
rs1878703
OSGEP
1 1.000 0.080 14 20452590 intron variant C/G;T snv 0.010 < 0.001 1 2015 2015
dbSNP: rs188212047
rs188212047
STXBP2
1 1.000 0.080 19 7642058 missense variant G/T snv 8.0E-05 3.5E-05 0.010 1.000 1 2017 2017
dbSNP: rs1998055
rs1998055
SLC7A8
1 1.000 0.080 14 23154618 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs2003334
rs2003334
ALDH1L1 ; SLC41A3 ; ALDH1L1-AS1 ; LOC112267887
1 1.000 0.080 3 126103160 upstream gene variant C/T snv 0.36 0.700 1.000 1 2011 2011