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: rs2272046
rs2272046
HMGA2
1.000 0.120 12 65830681 intron variant A/C snv 2.1E-02
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome 		0.810 1.000 1 2012 2018
dbSNP: rs1042725
rs1042725
HMGA2
0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.800 1.000 1 2013 2013
dbSNP: rs8756
rs8756
HMGA2
0.882 0.200 12 65965972 3 prime UTR variant C/A snv 0.56
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 6 2008 2019
dbSNP: rs1042725
rs1042725
HMGA2
0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 5 2007 2019
dbSNP: rs1351394
rs1351394
HMGA2
12 65958046 3 prime UTR variant T/C;G snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 3 2010 2019
dbSNP: rs7979673
rs7979673
HMGA2
12 65833477 intron variant C/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2011 2019
dbSNP: rs1042725
rs1042725
HMGA2
0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs10784502
rs10784502
HMGA2
12 65950030 intron variant C/T snv 0.53
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2017 2017
dbSNP: rs12371967
rs12371967
HMGA2
12 65952934 3 prime UTR variant T/C snv 0.12
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs1351394
rs1351394
HMGA2
12 65958046 3 prime UTR variant T/C;G snv
CUI: C0562350
Disease: Hip circumference
Hip circumference 		0.700 1.000 1 2015 2015
dbSNP: rs1351394
rs1351394
HMGA2
12 65958046 3 prime UTR variant T/C;G snv
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2016 2016
dbSNP: rs1351394
rs1351394
HMGA2
12 65958046 3 prime UTR variant T/C;G snv
CUI: C0419415
Disease: Birth length
Birth length 		0.700 1.000 1 2015 2015
dbSNP: rs1480474
rs1480474
HMGA2
1.000 0.080 12 65933163 intron variant A/G snv 0.45
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2018 2018
dbSNP: rs17179670
rs17179670
HMGA2
12 65956032 3 prime UTR variant A/G snv 0.16
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs189339
rs189339
HMGA2 ; HMGA2-AS1
12 65858514 non coding transcript exon variant A/G snv 0.72
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs2258238
rs2258238
HMGA2 ; RPSAP52
1.000 0.080 12 65827280 intron variant A/G;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2019 2019
dbSNP: rs343092
rs343092
HMGA2 ; HMGA2-AS1
1.000 0.080 12 65857160 non coding transcript exon variant T/G snv 0.63
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 1.000 1 2014 2014
dbSNP: rs73121716
rs73121716
HMGA2
12 65924437 intron variant C/T snv 1.1E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs76456255
rs76456255
HMGA2
1.000 12 65950114 intron variant C/A snv 6.5E-02
CUI: C0869220
Disease: Adverse effects, not elsewhere classified
Adverse effects, not elsewhere classified 		0.700 1.000 1 2019 2019
dbSNP: rs7970350
rs7970350
HMGA2
12 65966384 downstream gene variant C/T snv 0.48
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs7970350
rs7970350
HMGA2
12 65966384 downstream gene variant C/T snv 0.48
CUI: C0455806
Disease: Infant length
Infant length 		0.700 1.000 1 2015 2015
dbSNP: rs7970350
rs7970350
HMGA2
12 65966384 downstream gene variant C/T snv 0.48
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs7970350
rs7970350
HMGA2
12 65966384 downstream gene variant C/T snv 0.48
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		0.700 1.000 1 2017 2017
dbSNP: rs8756
rs8756
HMGA2
0.882 0.200 12 65965972 3 prime UTR variant C/A snv 0.56
CUI: C0005612
Disease: Birth Weight
Birth Weight 		0.700 1.000 1 2019 2019
dbSNP: rs8756
rs8756
HMGA2
0.882 0.200 12 65965972 3 prime UTR variant C/A snv 0.56
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE 		0.700 1.000 1 2019 2019