C1QTNF7, C1q and TNF related 7, 114905

N. diseases: 9; N. variants: 6
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs16891867
rs16891867 		1.000 0.040 4 15395740 intron variant A/G snv 0.11
CUI: C0149654
Disease: Conduct Disorder
Conduct Disorder 		Mental Disorders 0.800 1.000 1 2011 2011
dbSNP: rs1861046
rs1861046 		1.000 0.040 4 15396282 intron variant G/A snv 0.11
CUI: C0149654
Disease: Conduct Disorder
Conduct Disorder 		Mental Disorders 0.800 1.000 1 2011 2011
dbSNP: rs114133078
rs114133078 		4 15352761 intron variant T/C snv 2.9E-02
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.700 1.000 1 2013 2013
dbSNP: rs13102822
rs13102822 		4 15386753 intron variant G/A;C snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs4515160
rs4515160 		4 15382920 intron variant C/G snv 0.23
CUI: C4317009
Disease: Diverticular Diseases
Diverticular Diseases 		Digestive System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs6449133
rs6449133 		4 15378653 intron variant T/G snv 0.48
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2018 2018