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: rs141023293
rs141023293
1.000 0.120 11 116902201 intron variant G/A snv 1.5E-02
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder)
0.700 1.000 1 2018 2018
dbSNP: rs7115242
rs7115242
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.700 1.000 1 2016 2016
dbSNP: rs12099358
rs12099358
11 116855332 non coding transcript exon variant C/A snv 0.24
CUI: C0523522
Disease: beta-Endorphin measurement
beta-Endorphin measurement
0.700 1.000 1 2017 2017
dbSNP: rs77204473
rs77204473
11 116934348 intron variant T/C;G snv
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2016 2016
dbSNP: rs201462698
rs201462698
1.000 0.080 11 116897884 intron variant AA/-;A;AAA delins 8.4E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.700 1.000 1 2017 2017
dbSNP: rs7115242
rs7115242
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0011847
Disease: Diabetes
Diabetes
0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level
0.700 1.000 1 2016 2016
dbSNP: rs77204473
rs77204473
11 116934348 intron variant T/C;G snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs78692246
rs78692246
11 116920591 intron variant G/A snv 7.3E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs7115242
rs7115242
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0337438
Disease: Glucose measurement
Glucose measurement
0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0018801
Disease: Heart failure
Heart failure
0.700 1.000 1 2016 2016
dbSNP: rs7115242
rs7115242
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs11216230
rs11216230
11 117014073 intron variant G/A snv 3.1E-02
High density lipoprotein measurement
0.800 1.000 3 2014 2019
dbSNP: rs12225230
rs12225230
11 116857914 missense variant G/A;C;T snv 1.2E-05; 0.19; 4.0E-06
High density lipoprotein measurement
0.800 1.000 1 2012 2018
dbSNP: rs139961185
rs139961185
11 116936627 intron variant G/A snv 1.1E-02
High density lipoprotein measurement
0.700 1.000 1 2019 2019
dbSNP: rs7115242
rs7115242
0.851 0.120 11 117037567 intron variant A/G;T snv
High density lipoprotein measurement
0.700 1.000 1 2016 2016
dbSNP: rs7115583
rs7115583
11 116913660 intron variant G/T snv 0.17
High density lipoprotein measurement
0.700 1.000 1 2019 2019
dbSNP: rs7115242
rs7115242
0.851 0.120 11 117037567 intron variant A/G;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.700 1.000 1 2016 2016
dbSNP: rs10892044
rs10892044
1.000 0.040 11 116896183 intron variant T/C snv 0.16
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.700 1.000 1 2018 2018
dbSNP: rs11216186
rs11216186
1.000 0.040 11 116913976 intron variant T/C snv 7.5E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.700 1.000 1 2018 2018