SLC9A1, solute carrier family 9 member A1, 6548

N. diseases: 144; N. variants: 4
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: rs786204831
rs786204831 		1.000 1 27109678 missense variant C/T snv
CUI: C4225383
Disease: LICHTENSTEIN-KNORR SYNDROME
LICHTENSTEIN-KNORR SYNDROME 		0.800 0
dbSNP: rs11806219
rs11806219 		1 27121557 intron variant G/A snv 6.0E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11807614
rs11807614 		1 27138426 intron variant A/G snv 1.9E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs745927136
rs745927136 		1.000 0.120 1 27102734 missense variant G/A snv 4.0E-05
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2018 2018