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: rs10761779
rs10761779
JMJD1C
10 63515167 intron variant A/G snv 0.42
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement 		0.700 1.000 1 2008 2008
dbSNP: rs10822161
rs10822161
JMJD1C
10 63358443 intron variant G/A;T snv
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12355784
rs12355784
JMJD1C
10 63361805 intron variant C/A;T snv
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement 		0.700 1.000 1 2008 2008
dbSNP: rs7923609
rs7923609
JMJD1C ; MIR1296
10 63374062 intron variant A/G snv 0.43
CUI: C0201850
Disease: Alkaline phosphatase measurement
Alkaline phosphatase measurement 		0.800 1.000 1 2011 2011
dbSNP: rs75446656
rs75446656
JMJD1C
1.000 0.080 10 63340256 intron variant C/A;T snv
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2017 2017
dbSNP: rs1935
rs1935
JMJD1C
10 63168063 missense variant C/A;G;T snv 4.0E-06; 0.44
CUI: C0242216
Disease: Biliary calculi
Biliary calculi 		0.700 1.000 1 2018 2018
dbSNP: rs10822168
rs10822168
JMJD1C
10 63405424 intron variant G/A snv 0.43
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7896518
rs7896518
JMJD1C
10 63344740 intron variant A/G snv 0.38
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs7080386
rs7080386
JMJD1C
10 63288546 intron variant C/A snv 0.38
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7916868
rs7916868
JMJD1C
10 63229171 intron variant A/T snv 0.47
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs7924036
rs7924036
JMJD1C
10 63431885 intron variant G/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs34044188
rs34044188
JMJD1C
1.000 0.080 10 63497603 intron variant C/A;T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs35632171
rs35632171
JMJD1C
1.000 0.080 10 63349742 intron variant T/G snv 2.8E-02
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs35997229
rs35997229
JMJD1C
1.000 0.080 10 63197831 intron variant T/C;G snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs10761731
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2016 2016
dbSNP: rs10995477
rs10995477
JMJD1C
10 63250912 intron variant T/C snv 0.43
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs7916868
rs7916868
JMJD1C
10 63229171 intron variant A/T snv 0.47
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.700 1.000 2 2016 2017
dbSNP: rs10761756
rs10761756
JMJD1C
10 63412568 intron variant C/T snv 0.42
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.700 1.000 1 2017 2017
dbSNP: rs7896783
rs7896783
JMJD1C
10 63402393 intron variant G/A;C snv
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.800 1.000 1 2013 2013
dbSNP: rs7082066
rs7082066
JMJD1C
10 63239211 intron variant A/G snv 0.69
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2019 2019
dbSNP: rs7899503
rs7899503
JMJD1C
10 63327708 intron variant C/G;T snv
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2018 2018
dbSNP: rs10995477
rs10995477
JMJD1C
10 63250912 intron variant T/C snv 0.43
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs10761731
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2016 2016
dbSNP: rs10761733
rs10761733
JMJD1C
10 63275024 intron variant T/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs10761739
rs10761739
JMJD1C
10 63302248 intron variant G/C snv 0.38
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019