Source: GWASCAT

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 2 2013 2018
dbSNP: rs16856332
rs16856332
ABCB11
2 168984064 intron variant T/A;G snv
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement 		0.800 1.000 1 2011 2011
dbSNP: rs563694
rs563694
ABCB11
2 168917561 intron variant C/A snv 0.75
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		0.800 1.000 1 2008 2008
dbSNP: rs569805
rs569805
ABCB11
1.000 0.040 2 168926370 intron variant A/T snv 0.73
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.800 1.000 1 2011 2011
dbSNP: rs853789
rs853789
ABCB11
2 168944978 intron variant A/G;T snv 0.75
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		0.800 1.000 1 2012 2018
dbSNP: rs16856247
rs16856247
ABCB11
2 168927903 intron variant C/T snv 6.6E-02
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		0.700 1.000 3 2011 2019
dbSNP: rs10176901
rs10176901
ABCB11
2 168974151 intron variant G/A snv 0.57
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 2 2019 2019
dbSNP: rs10176901
rs10176901
ABCB11
2 168974151 intron variant G/A snv 0.57
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2019 2019
dbSNP: rs10177080
rs10177080
ABCB11
2 168974288 intron variant G/A snv 0.53
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2241339
rs2241339
ABCB11
2 169013785 intron variant C/A;T snv
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2241339
rs2241339
ABCB11
2 169013785 intron variant C/A;T snv
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2241339
rs2241339
ABCB11
2 169013785 intron variant C/A;T snv
CUI: C0201899
Disease: Aspartate aminotransferase measurement
Aspartate aminotransferase measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2287621
rs2287621
ABCB11
2 168974005 intron variant G/A snv 0.66
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2287621
rs2287621
ABCB11
2 168974005 intron variant G/A snv 0.66
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2287622
rs2287622
ABCB11
0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2017 2017
dbSNP: rs2287623
rs2287623
ABCB11
2 168973645 intron variant G/A snv 0.57
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2389606
rs2389606
ABCB11
2 168973262 intron variant C/T snv 0.57
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs3770585
rs3770585
ABCB11
2 168967357 intron variant G/A;C snv 0.40
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs3770585
rs3770585
ABCB11
2 168967357 intron variant G/A;C snv 0.40
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs72623176
rs72623176
ABCB11
2 168977860 intron variant G/A snv 7.5E-02
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7576531
rs7576531
ABCB11
1.000 0.080 2 168969959 intron variant C/T snv 3.8E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2018 2018
dbSNP: rs853789
rs853789
ABCB11
2 168944978 intron variant A/G;T snv 0.75
CUI: C0017741
Disease: Glucose tolerance test
Glucose tolerance test 		0.700 1.000 1 2018 2018