STK39, serine/threonine kinase 39, 27347

N. diseases: 38; N. variants: 7
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: rs6749447
rs6749447
2 168184876 intron variant T/G snv 0.37
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
0.800 1.000 1 2009 2009
dbSNP: rs2390669
rs2390669
1.000 0.040 2 168235432 intron variant A/C snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs2390669
rs2390669
1.000 0.040 2 168235432 intron variant A/C snv 0.14
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs3754777
rs3754777
1.000 0.040 2 168159404 intron variant C/T snv 0.16
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.060 0.833 6 2012 2019
dbSNP: rs35929607
rs35929607
2 168179226 intron variant A/G snv 0.27
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.030 0.667 3 2011 2016
dbSNP: rs6749447
rs6749447
2 168184876 intron variant T/G snv 0.37
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.030 0.667 3 2013 2018
dbSNP: rs1517342
rs1517342
1.000 0.040 2 168159163 intron variant T/C snv 0.50
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs3754775
rs3754775
1.000 0.040 2 168159753 intron variant C/T snv 0.16
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs3754777
rs3754777
1.000 0.040 2 168159404 intron variant C/T snv 0.16
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs6433027
rs6433027
2 168007850 intron variant T/C snv 0.49
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 1.000 1 2012 2012