CLCN6, chloride voltage-gated channel 6, 1185

N. diseases: 24; N. variants: 25
Disease: Hypertensive disease ×
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: rs5063
rs5063 		0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.060 1.000 6 2007 2019
dbSNP: rs5065
rs5065 		0.763 0.240 1 11846011 stop lost A/G snv 0.14 0.21
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.030 1.000 3 2007 2011
dbSNP: rs5068
rs5068 		0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.030 1.000 3 2009 2017
dbSNP: rs198358
rs198358 		0.925 0.040 1 11844019 3 prime UTR variant T/C snv 0.32
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.020 1.000 2 2009 2011
dbSNP: rs13306560
rs13306560 		1.000 0.040 1 11806126 5 prime UTR variant C/T snv 3.7E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015