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: 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: rs7896518
rs7896518
JMJD1C
10 63344740 intron variant A/G snv 0.38
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 3 2012 2019
dbSNP: rs7075195
rs7075195
JMJD1C
10 63290899 intron variant A/G snv 0.38
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 2 2011 2014
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: 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: 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: rs7082066
rs7082066
JMJD1C
10 63239211 intron variant A/G snv 0.69
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
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: rs7896518
rs7896518
JMJD1C
10 63344740 intron variant A/G snv 0.38
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2017 2017
dbSNP: rs7896518
rs7896518
JMJD1C
10 63344740 intron variant A/G snv 0.38
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
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: 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: rs9415676
rs9415676
JMJD1C
10 63250866 intron variant A/G snv 0.44
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 1 2019 2019
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: 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: rs10995505
rs10995505
JMJD1C
10 63331399 intron variant A/G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs10761731
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 4 2010 2019
dbSNP: rs10761731
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.800 1.000 3 2011 2019
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: 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: 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: rs10761731
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38
CUI: C2697760
Disease: Interleukin 12 Measurement
Interleukin 12 Measurement 		0.700 1.000 1 2017 2017