Gene: SCARB1 ×
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: rs838880
rs838880
SCARB1
3 12 124777047 3 prime UTR variant C/T snv 0.55 0.800 1.000 4 2010 2019
dbSNP: rs10773112
rs10773112
SCARB1
2 12 124853983 intron variant C/T snv 0.63 0.800 1.000 3 2012 2019
dbSNP: rs10773105
rs10773105
SCARB1
2 12 124799220 intron variant C/T snv 0.63 0.800 1.000 2 2012 2019
dbSNP: rs10846743
rs10846743
SCARB1
2 12 124825759 intron variant G/A snv 3.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs12580323
rs12580323
SCARB1
2 12 124795115 intron variant C/T snv 1.5E-02 0.700 1.000 1 2012 2012
dbSNP: rs12819677
rs12819677
SCARB1
2 12 124798975 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs57276302
rs57276302
SCARB1 ; LOC107984444
2 12 124879441 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs61005347
rs61005347
SCARB1
1 12 124841232 intron variant C/T snv 2.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs67053123
rs67053123
SCARB1 ; LOC105370050
2 12 124869264 intron variant T/A snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs7137923
rs7137923
SCARB1
2 12 124822302 intron variant G/T snv 3.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs78194510
rs78194510
SCARB1
2 1.000 0.080 12 124853790 intron variant T/C snv 8.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs838886
rs838886
SCARB1
1 12 124779741 intron variant T/A;G snv 0.700 1.000 1 2015 2015
dbSNP: rs865716
rs865716
SCARB1
2 12 124806310 intron variant A/T snv 0.58 0.700 1.000 1 2012 2012