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: rs10248619
rs10248619
GRB10
7 50683393 intron variant T/C snv 0.71
CUI: C1305855
Disease: Body mass index
Body mass index 		0.800 1.000 1 2012 2012
dbSNP: rs12540874
rs12540874
GRB10
0.882 0.280 7 50597225 intron variant A/C;G snv
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.800 1.000 1 2011 2011
dbSNP: rs10248619
rs10248619
GRB10
7 50683393 intron variant T/C snv 0.71
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10275663
rs10275663
GRB10
7 50729988 intron variant G/A snv 9.4E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2015 2015
dbSNP: rs10275663
rs10275663
GRB10
7 50729988 intron variant G/A snv 9.4E-02
CUI: C1305849
Disease: Diastolic blood pressure measurement
Diastolic blood pressure measurement 		0.700 1.000 1 2015 2015
dbSNP: rs10486757
rs10486757
GRB10
7 50626161 intron variant G/A snv 8.8E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs11555134
rs11555134
GRB10
7 50591496 3 prime UTR variant C/T snv 0.22
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs145761614
rs145761614
GRB10
7 50708789 intron variant C/T snv 7.2E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs17152083
rs17152083
GRB10
7 50671913 intron variant G/C snv 8.9E-02
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs17548938
rs17548938
GRB10
7 50739728 intron variant G/A snv 8.3E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs17548938
rs17548938
GRB10
7 50739728 intron variant G/A snv 8.3E-02
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs2237467
rs2237467
GRB10
7 50665619 intron variant G/A snv 0.19
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2019 2019
dbSNP: rs2529411
rs2529411
GRB10
7 50670785 intron variant G/C snv 0.66
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs2715135
rs2715135
GRB10
7 50682431 intron variant T/G snv 0.68
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs6976572
rs6976572
GRB10
7 50772101 intron variant C/T snv 0.46
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs73116822
rs73116822
GRB10
7 50670155 intron variant C/T snv 9.0E-02
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs73116829
rs73116829
GRB10
7 50672041 intron variant G/A snv 7.4E-02
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs933360
rs933360
GRB10
7 50690548 intron variant C/T snv 0.60
CUI: C0202098
Disease: Insulin measurement
Insulin measurement 		0.700 1.000 1 2014 2014
dbSNP: rs933360
rs933360
GRB10
7 50690548 intron variant C/T snv 0.60
CUI: C4049919
Disease: Insulin Sensitivity Measurement
Insulin Sensitivity Measurement 		0.700 1.000 1 2014 2014
dbSNP: rs9656664
rs9656664
GRB10
7 50594275 intron variant A/G snv 0.17
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019