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: rs2893923
rs2893923
JMJD1C
10 63501424 intron variant C/T snv 0.27
CUI: C2697760
Disease: Interleukin 12 Measurement
Interleukin 12 Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs34524635
rs34524635
JMJD1C
10 63501417 intron variant T/- delins 0.43
CUI: C2239222
Disease: Vascular Endothelial Growth Factor Measurement
Vascular Endothelial Growth Factor Measurement 		0.700 1.000 1 2017 2017
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: rs10740128
rs10740128
JMJD1C
10 63490783 intron variant A/G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs7085862
rs7085862
JMJD1C
10 63486687 intron variant T/G snv 0.66
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs3999089
rs3999089
JMJD1C
10 63444048 intron variant A/G snv 0.41
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs3999089
rs3999089
JMJD1C
10 63444048 intron variant A/G snv 0.41
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7924036
rs7924036
JMJD1C
10 63431885 intron variant G/A;T snv
CUI: C0337443
Disease: Sodium measurement
Sodium measurement 		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: rs7924036
rs7924036
JMJD1C
10 63431885 intron variant G/A;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs10761765
rs10761765
JMJD1C ; LOC105378330
10 63429213 intron variant A/G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs6479901
rs6479901
JMJD1C
10 63421016 intron variant C/A snv 0.66
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
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: 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: 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: rs4745706
rs4745706
JMJD1C
10 63399820 intron variant T/C snv 0.13
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs10761751
rs10761751
JMJD1C
10 63395125 intron variant A/G snv 0.42
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs7910927
rs7910927
JMJD1C
10 63379150 intron variant T/A;G snv
CUI: C0202218
Disease: Sex hormone binding globulin measurement
Sex hormone binding globulin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2893919
rs2893919
JMJD1C ; MIR1296
10 63375018 intron variant G/A snv 0.43
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2019 2019
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: rs2393967
rs2393967
JMJD1C ; MIR1296
10 63373396 intron variant A/C snv 0.23
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs2393967
rs2393967
JMJD1C ; MIR1296
10 63373396 intron variant A/C snv 0.23
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2009 2012
dbSNP: rs2393967
rs2393967
JMJD1C ; MIR1296
10 63373396 intron variant A/C snv 0.23
CUI: C2697760
Disease: Interleukin 12 Measurement
Interleukin 12 Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs10761750
rs10761750
JMJD1C
10 63368859 intron variant G/A snv 0.43
CUI: C2239222
Disease: Vascular Endothelial Growth Factor Measurement
Vascular Endothelial Growth Factor Measurement 		0.700 1.000 1 2017 2017