Gene: ABCB11 ×
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: rs10176901
rs10176901
ABCB11
2 2 168974151 intron variant G/A snv 0.57 0.700 1.000 2 2019 2019
dbSNP: rs11568373
rs11568373
ABCB11
3 2 168944893 synonymous variant T/C snv 5.8E-03 2.6E-02 0.700 1.000 1 2012 2012
dbSNP: rs16856314
rs16856314
ABCB11
3 2 168966582 intron variant G/A snv 3.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs2287621
rs2287621
ABCB11
2 2 168974005 intron variant G/A snv 0.66 0.700 1.000 1 2018 2018
dbSNP: rs2287623
rs2287623
ABCB11
2 2 168973645 intron variant G/A snv 0.57 0.700 1.000 1 2018 2018
dbSNP: rs2389606
rs2389606
ABCB11
1 2 168973262 intron variant C/T snv 0.57 0.700 1.000 1 2018 2018
dbSNP: rs6709971
rs6709971
ABCB11
3 2 169011063 intron variant T/C snv 2.6E-02 0.700 1.000 1 2012 2012