CHD7 Chromosome 8

Chromodomain helicase DNA binding protein 7
1096 variants 1096 Health Risk

Upload your DNA to see your personal genotypes for variants in CHD7.

What This Gene Does
This gene encodes a protein that contains several helicase family domains. Mutations in this gene have been found in some patients with the CHARGE syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]
Gene Info
Gene Group
"Myb/SANT domain containing|Helicases|SNF2 related family"
Locus Type
gene with protein product
Location
8q12.2
Ensembl
ENSG00000171316
Associated Conditions (46)
CHARGE syndrome
Hypogonadotropic hypogonadism 5 with or without anosmia
Inborn genetic diseases
CHD7-related disorder
Uterine corpus endometrial carcinoma
Male infertility with spermatogenesis disorder
See cases
Familial atrioventricular septal defect
3MC syndrome
Amenorrhea
Childhood onset hearing loss
CHD7-related CHARGE syndrome
Cleft palate
Lung cancer
Hearing impairment
3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency
Intellectual disability
Primary dilated cardiomyopathy
Neurodevelopmental disorder
Congenital heart disease
+26 more conditions
Key Variants
RS1001403179
Conflicting classifications of pathogenicity
CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia, CHARGE syndrome
Health Risk
RS1012221437
Conflicting classifications of pathogenicity
CHARGE syndrome, Inborn genetic diseases, Hypogonadotropic hypogonadism 5 with or without anosmia
Health Risk
RS1020281061
Conflicting classifications of pathogenicity
CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia, CHARGE syndrome
Health Risk
RS1024797402
Conflicting classifications of pathogenicity
CHARGE syndrome, CHARGE syndrome
Health Risk
RS1032877391
Conflicting classifications of pathogenicity
CHARGE syndrome, CHD7-related disorder, CHARGE syndrome
Health Risk
RS1046787337
Conflicting classifications of pathogenicity
CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia, Inborn genetic diseases
Health Risk
RS1060503188
Conflicting classifications of pathogenicity
CHARGE syndrome, CHARGE syndrome, CHARGE syndrome
Health Risk
RS1064793083
Conflicting classifications of pathogenicity
Inborn genetic diseases, Hypogonadotropic hypogonadism 5 with or without anosmia, CHARGE syndrome
Health Risk
RS1064794548
Conflicting classifications of pathogenicity
CHARGE syndrome, CHARGE syndrome
Health Risk
RS1064794649
Conflicting classifications of pathogenicity
CHARGE syndrome, CHD7-related disorder, CHARGE syndrome
Health Risk
RS1064794854
Conflicting classifications of pathogenicity
CHARGE syndrome, CHARGE syndrome
Health Risk
RS1064795809
Conflicting classifications of pathogenicity
Inborn genetic diseases, CHARGE syndrome, Inborn genetic diseases
Health Risk
All Variants (1096)
RSID Category Clinical Significance Conditions
RS2150669783 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150669923 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150669944 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150669971 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150670337 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150697457 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150697555 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150697787 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150697832 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150708627 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150708828 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150708918 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150723965 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150748709 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150748939 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150749363 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150749475 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150750228 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150752540 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150752695 Health Risk Pathogenic
RS2150761158 Health Risk Pathogenic CHARGE syndrome, CHD7-related disorder, CHARGE syndrome
RS2150764898 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150776997 Health Risk Pathogenic
RS2150777148 Health Risk Pathogenic CHD7 disorder, CHD7 disorder
RS2150777291 Health Risk Pathogenic
RS2150779252 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150779267 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150785999 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150786107 Health Risk Pathogenic
RS2150786214 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150786530 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150792975 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150793053 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150793143 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150793975 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150801705 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150804625 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150805748 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150806303 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150807513 Health Risk Pathogenic
RS2150808082 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150808631 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150808654 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150808678 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150808685 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150809140 Health Risk Pathogenic
RS2150809777 Health Risk Pathogenic CHARGE syndrome, CHD7-related disorder, CHARGE syndrome
RS2150809927 Health Risk Pathogenic CHARGE syndrome, Inborn genetic diseases, CHARGE syndrome
RS2150810800 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS2150811163 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
« Prev 1 ... 14 15 16 17 18 19 20 ... 22 Next »
Sign Up to Analyze Your DNA Log In