Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2287623
rs2287623
ABCB11
2 168973645 intron variant G/A snv 0.57
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 1 2013 2018
dbSNP: rs11568373
rs11568373
ABCB11
2 168944893 synonymous variant T/C snv 5.8E-03 2.6E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs16856314
rs16856314
ABCB11
2 168966582 intron variant G/A snv 3.0E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs6709971
rs6709971
ABCB11
2 169011063 intron variant T/C snv 2.6E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012