NLGN4X, neuroligin 4 X-linked, 57502

N. diseases: 6; N. variants: 6
Source: CURATED ×
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: rs12009217
rs12009217 		1.000 0.040 X 6002841 intron variant A/G snv 0.28
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs12845396
rs12845396 		1.000 0.040 X 6111492 intron variant A/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs1569118680
rs1569118680 		0.925 0.080 X 5903423 frameshift variant TC/- delins
CUI: C1845539
Disease: AUTISM, X-LINKED, SUSCEPTIBILITY TO, 2 (finding)
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 2 (finding) 		0.700 0
dbSNP: rs1569118680
rs1569118680 		0.925 0.080 X 5903423 frameshift variant TC/- delins
CUI: C3501611
Disease: Mental Retardation, X-Linked Nonsyndromic
Mental Retardation, X-Linked Nonsyndromic 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.700 0
dbSNP: rs1569118853
rs1569118853 		0.925 X 5903492 frameshift variant -/A delins
CUI: C1845334
Disease: ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2 (finding)
ASPERGER SYNDROME, X-LINKED, SUSCEPTIBILITY TO, 2 (finding) 		0.700 0
dbSNP: rs1569118853
rs1569118853 		0.925 X 5903492 frameshift variant -/A delins
CUI: C1845539
Disease: AUTISM, X-LINKED, SUSCEPTIBILITY TO, 2 (finding)
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 2 (finding) 		0.700 0
dbSNP: rs749477993
rs749477993 		1.000 0.080 X 5909225 missense variant C/T snv 1.6E-05 9.5E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs756651509
rs756651509 		1.000 X 6151166 stop gained G/A snv
CUI: C1845539
Disease: AUTISM, X-LINKED, SUSCEPTIBILITY TO, 2 (finding)
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 2 (finding) 		0.700 0