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: 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: 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: 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: rs10995477
rs10995477
JMJD1C
10 63250912 intron variant T/C snv 0.43
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
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: rs10995477
rs10995477
JMJD1C
10 63250912 intron variant T/C snv 0.43
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		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: rs10995505
rs10995505
JMJD1C
10 63331399 intron variant A/G;T snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
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: rs143014767
rs143014767
JMJD1C
10 63304077 intron variant CTTTGCC/- del
CUI: C2825877
Disease: Interferon Gamma Measurement
Interferon Gamma Measurement 		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: 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: C2697760
Disease: Interleukin 12 Measurement
Interleukin 12 Measurement 		0.700 1.000 1 2017 2017
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: 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: 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: 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: 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: 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: rs41274072
rs41274072
JMJD1C
10 63214396 missense variant T/C snv 2.9E-02 5.3E-02
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs4454603
rs4454603
JMJD1C
10 63252990 intron variant C/T snv 0.43
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2018 2018
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