Source: ALL

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: rs3810291
rs3810291
19 47065746 3 prime UTR variant G/A snv 0.50
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 10 2010 2019
dbSNP: rs3810291
rs3810291
19 47065746 3 prime UTR variant G/A snv 0.50
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index
0.700 1.000 3 2010 2014
dbSNP: rs3810291
rs3810291
19 47065746 3 prime UTR variant G/A snv 0.50
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure
0.700 1.000 3 2010 2014
dbSNP: rs10408163
rs10408163
19 47093845 non coding transcript exon variant T/C snv 0.52
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
0.700 1.000 1 2017 2017
dbSNP: rs10408163
rs10408163
19 47093845 non coding transcript exon variant T/C snv 0.52
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs10408163
rs10408163
19 47093845 non coding transcript exon variant T/C snv 0.52
High density lipoprotein measurement
0.700 1.000 1 2018 2018
dbSNP: rs10408163
rs10408163
19 47093845 non coding transcript exon variant T/C snv 0.52
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs10408163
rs10408163
19 47093845 non coding transcript exon variant T/C snv 0.52
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs10408163
rs10408163
19 47093845 non coding transcript exon variant T/C snv 0.52
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs113125564
rs113125564
19 47092874 intron variant T/C snv 2.9E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs12973221
rs12973221
19 47111403 intron variant C/A snv 7.6E-02
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs12973221
rs12973221
19 47111403 intron variant C/A snv 7.6E-02
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs17716478
rs17716478
19 47097336 intron variant C/T snv 5.3E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs2241388
rs2241388
19 47069730 intron variant T/C snv 0.62
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2016 2016
dbSNP: rs2241388
rs2241388
19 47069730 intron variant T/C snv 0.62
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs2303108
rs2303108
19 47086638 intron variant T/C snv 0.63
High density lipoprotein measurement
0.700 1.000 1 2017 2017
dbSNP: rs2303108
rs2303108
19 47086638 intron variant T/C snv 0.63
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
0.700 1.000 1 2017 2017
dbSNP: rs2303108
rs2303108
19 47086638 intron variant T/C snv 0.63
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs3810291
rs3810291
19 47065746 3 prime UTR variant G/A snv 0.50
CUI: C0424678
Disease: Lean body mass
Lean body mass
0.700 1.000 1 2019 2019
dbSNP: rs3810291
rs3810291
19 47065746 3 prime UTR variant G/A snv 0.50
CUI: C0562350
Disease: Hip circumference
Hip circumference
0.700 1.000 1 2015 2015
dbSNP: rs3810291
rs3810291
19 47065746 3 prime UTR variant G/A snv 0.50
CUI: C1314691
Disease: Age at menarche
Age at menarche
0.700 1.000 1 2019 2019
dbSNP: rs3810291
rs3810291
19 47065746 3 prime UTR variant G/A snv 0.50
CUI: C0455829
Disease: Waist Circumference
Waist Circumference
0.700 1.000 1 2015 2015
dbSNP: rs3810291
rs3810291
19 47065746 3 prime UTR variant G/A snv 0.50
CUI: C0037369
Disease: Smoking
Smoking
0.700 1.000 1 2017 2017
dbSNP: rs3810291
rs3810291
19 47065746 3 prime UTR variant G/A snv 0.50
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
0.700 1.000 1 2017 2017
dbSNP: rs62135070
rs62135070
19 47112578 missense variant C/T snv 3.7E-02 3.1E-02
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019