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: rs2373115
rs2373115
0.925 0.080 11 78380104 intron variant C/A snv 0.24
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.900 0.750 1 2007 2018
dbSNP: rs10899489
rs10899489
11 78384327 non coding transcript exon variant C/A;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.800 1.000 1 2010 2010
dbSNP: rs7107174
rs7107174
1.000 0.120 11 78286890 intron variant C/G;T snv
CUI: C1336708
Disease: Testicular Germ Cell Tumor
Testicular Germ Cell Tumor
0.710 1.000 1 2015 2015
dbSNP: rs10793308
rs10793308
11 78374959 intron variant C/T snv 0.26
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2018 2018
dbSNP: rs10793310
rs10793310
11 78387968 intron variant T/G snv 0.15
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs10899469
rs10899469
11 78307267 intron variant T/C snv 0.15
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs11237450
rs11237450
11 78312310 intron variant C/A snv 0.15
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2019 2019
dbSNP: rs11237485
rs11237485
11 78414965 intron variant G/A snv 0.16
CUI: C0201973
Disease: Creatine kinase measurement
Creatine kinase measurement
0.700 1.000 1 2018 2018
dbSNP: rs1981405
rs1981405
11 78265162 intron variant C/G;T snv
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs2063730
rs2063730
11 78337478 intron variant A/C;G snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2014 2014
dbSNP: rs2292572
rs2292572
11 78341818 5 prime UTR variant G/A;T snv
CUI: C0018498
Disease: Hair Color
Hair Color
0.700 1.000 1 2018 2018
dbSNP: rs2450128
rs2450128
11 78229029 intron variant G/A snv 0.25
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs2511158
rs2511158
11 78262934 intron variant C/T snv 0.15
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs2511162
rs2511162
11 78216055 3 prime UTR variant A/G snv 0.31
Creatinine measurement, serum (procedure)
0.700 1.000 1 2018 2018
dbSNP: rs2512519
rs2512519
1.000 0.040 11 78241969 intron variant C/T snv 0.18
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.700 1.000 1 2019 2019
dbSNP: rs2512519
rs2512519
1.000 0.040 11 78241969 intron variant C/T snv 0.18
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE
0.700 1.000 1 2019 2019
dbSNP: rs4945275
rs4945275
11 78408776 intron variant G/A;C snv
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2018 2018
dbSNP: rs7939352
rs7939352
11 78292105 intron variant G/A snv 0.27
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs7939352
rs7939352
11 78292105 intron variant G/A snv 0.27
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs7939352
rs7939352
11 78292105 intron variant G/A snv 0.27
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs7939352
rs7939352
11 78292105 intron variant G/A snv 0.27
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018