TNNI3K, TNNI3 interacting kinase, 51086

N. diseases: 50; N. variants: 23
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: rs1040070
rs1040070 		1.000 0.080 1 74512186 intron variant G/A;C snv
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2016 2016
dbSNP: rs7514705
rs7514705 		1 74541036 intron variant T/C snv 0.41
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2014 2014
dbSNP: rs7553348
rs7553348 		1 74539383 intron variant G/A snv 0.42
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs12566985
rs12566985 		1 74536509 intron variant G/A snv 0.42
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 4 2015 2017
dbSNP: rs1514175
rs1514175 		1.000 0.080 1 74525960 intron variant A/G snv 0.48
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2010 2013
dbSNP: rs12041852
rs12041852 		1 74537816 intron variant G/A snv 0.41
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2016 2016
dbSNP: rs12042908
rs12042908 		1 74532078 intron variant A/G snv 0.41
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2018 2018
dbSNP: rs1514174
rs1514174 		1.000 0.080 1 74527379 intron variant C/T snv 0.44
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2015 2015
dbSNP: rs1514177
rs1514177 		1.000 0.080 1 74525718 intron variant C/G snv 0.49
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs7526762
rs7526762 		1 74527634 intron variant A/G snv 0.42
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs7551507
rs7551507 		1 74529541 intron variant C/T snv 0.41
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs7553158
rs7553158 		1 74539554 intron variant G/A snv 0.43
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs7553348
rs7553348 		1 74539383 intron variant G/A snv 0.42
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2015 2015
dbSNP: rs953567
rs953567 		1 74511741 intron variant A/G snv 0.42
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs1514175
rs1514175 		1.000 0.080 1 74525960 intron variant A/G snv 0.48
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 3 2010 2013
dbSNP: rs113313252
rs113313252 		1 74534327 intron variant -/T delins
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 1 2013 2013
dbSNP: rs12142020
rs12142020 		1 74534327 intron variant A/T snv 0.50
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 1 2013 2013
dbSNP: rs201167096
rs201167096 		1 74534327 intron variant -/T delins
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		0.700 1.000 1 2013 2013
dbSNP: rs606231469
rs606231469 		1.000 1 74369495 missense variant G/A snv
CUI: C4015285
Disease: CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY
CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY 		0.800 1.000 1 2011 2011
dbSNP: rs202238194
rs202238194 		1.000 1 74492217 missense variant G/A;C snv 1.6E-05
CUI: C4015285
Disease: CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY
CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY 		0.700 0
dbSNP: rs202238194
rs202238194 		1.000 1 74492217 missense variant G/A;C snv 1.6E-05
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs1514175
rs1514175 		1.000 0.080 1 74525960 intron variant A/G snv 0.48
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.700 1.000 3 2010 2013
dbSNP: rs113313252
rs113313252 		1 74534327 intron variant -/T delins
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.700 1.000 1 2013 2013
dbSNP: rs12142020
rs12142020 		1 74534327 intron variant A/T snv 0.50
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.700 1.000 1 2013 2013
dbSNP: rs201167096
rs201167096 		1 74534327 intron variant -/T delins
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		0.700 1.000 1 2013 2013