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: rs10773112
rs10773112
SCARB1
2 12 124853983 intron variant C/T snv 0.63 0.700 1.000 1 2012 2012
dbSNP: rs10818782
rs10818782
GABBR2
2 9 98325004 intron variant G/A snv 0.60 0.700 1.000 1 2013 2013
dbSNP: rs10846743
rs10846743
SCARB1
2 12 124825759 intron variant G/A snv 3.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs10891841
rs10891841
CADM1
2 11 115361021 intron variant T/G snv 1.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs10940493
rs10940493
IL6ST
2 5 55942083 intron variant C/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs10954843
rs10954843
NRG1
2 8 32419595 intron variant G/A snv 0.97 0.700 1.000 1 2012 2012
dbSNP: rs11035019
rs11035019
MMP26
2 11 4988333 intron variant C/T snv 2.6E-03 1.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs11065633
rs11065633
ATP2A2
2 12 110348445 3 prime UTR variant C/T snv 2.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs11216230
rs11216230
SIK3
2 11 117014073 intron variant G/A snv 3.1E-02 0.700 1.000 1 2014 2014
dbSNP: rs11217785
rs11217785
POU2F3 ; LOC105369531
2 11 120281882 intron variant C/T snv 0.33 0.700 1.000 1 2013 2013
dbSNP: rs11236530
rs11236530
DGAT2
2 11 75778359 intron variant C/A snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs11246602
rs11246602 		2 11 54607190 upstream gene variant A/G snv 0.11 0.700 1.000 1 2013 2013
dbSNP: rs1138429
rs1138429
SLC12A3
2 16 56909009 intron variant A/T snv 8.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs1144041
rs1144041
HMBS
2 11 119088570 intron variant T/C snv 9.9E-02 0.700 1.000 1 2012 2012
dbSNP: rs11555832
rs11555832
HMOX1
2 22 35393876 3 prime UTR variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11568026
rs11568026
AGT
2 1 230711777 intron variant A/G snv 3.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs11804107
rs11804107
SLC16A1
2 1 112929525 intron variant C/A snv 1.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs11819350
rs11819350 		2 10 17133943 upstream gene variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11833801
rs11833801
ADGRD1 ; LOC107984452
2 12 131076849 missense variant G/A;C snv 6.1E-03; 8.0E-06 0.700 1.000 1 2012 2012
dbSNP: rs11850375
rs11850375
ESR2
2 14 64244659 intron variant C/T snv 4.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs11875522
rs11875522
SMAD4
2 18 51065392 intron variant G/A snv 1.1E-02 4.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs11875600
rs11875600
LIPG
2 18 49572816 intron variant A/G snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs11938688
rs11938688
HPGDS
2 4 94336456 intron variant C/G snv 4.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs11941250
rs11941250
HPGDS
2 4 94308312 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs11960235
rs11960235
ADAMTS6
2 5 65451686 intron variant T/C snv 3.1E-02 0.700 1.000 1 2012 2012