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
RS199675125 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Inborn genetic diseases, CHARGE syndrome
RS199828744 Health Risk Conflicting classifications of pathogenicity Hypogonadotropic hypogonadism 5 with or without anosmia, CHARGE syndrome, Inborn genetic diseases
RS199919181 Health Risk Conflicting classifications of pathogenicity Hypogonadotropic hypogonadism 5 with or without anosmia, CHARGE syndrome, Inborn genetic diseases
RS199966549 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, CHARGE syndrome
RS200006916 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia
RS200220845 Health Risk Conflicting classifications of pathogenicity Hypogonadotropic hypogonadism 5 with or without anosmia, CHARGE syndrome, CHD7-related disorder
RS200277422 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Inborn genetic diseases, CHARGE syndrome
RS200441929 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Amenorrhea, Inborn genetic diseases
RS200565677 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Inborn genetic diseases, Hypogonadotropic hypogonadism 5 with or without anosmia
RS200644351 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia, Inborn genetic diseases
RS200806228 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia, Inborn genetic diseases
RS200898742 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, CHARGE syndrome
RS200907656 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, CHARGE syndrome, Inborn genetic diseases
RS201032343 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia, Inborn genetic diseases
RS201083157 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, CHD7-related disorder, Inborn genetic diseases
RS201423234 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Inborn genetic diseases, CHD7-related disorder
RS201456469 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Inborn genetic diseases, CHARGE syndrome
RS201470035 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia, Inborn genetic diseases
RS201514840 Health Risk Conflicting classifications of pathogenicity Hypogonadotropic hypogonadism 5 with or without anosmia, CHARGE syndrome, Inborn genetic diseases
RS201542180 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia, Inborn genetic diseases
RS201769233 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia, CHARGE syndrome
RS201793562 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Inborn genetic diseases, CHARGE syndrome
RS202039728 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia, CHARGE syndrome
RS202141372 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia, Inborn genetic diseases
RS202143667 Health Risk Conflicting classifications of pathogenicity Hypogonadotropic hypogonadism 5 with or without anosmia, Childhood onset hearing loss, CHARGE syndrome
RS202208393 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, CHD7-related disorder, Inborn genetic diseases
RS2129651419 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia, CHARGE syndrome
RS2150578971 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Inborn genetic diseases, Hypogonadotropic hypogonadism 5 with or without anosmia
RS2150723994 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia, CHARGE syndrome
RS2150779357 Health Risk Conflicting classifications of pathogenicity CHD7-related disorder, CHD7-related disorder
RS2150805872 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, CHARGE syndrome
RS2150810874 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, CHD7-related disorder, CHARGE syndrome
RS2487672040 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, CHARGE syndrome
RS2487971762 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, CHD7-related CHARGE syndrome, CHARGE syndrome
RS2487976511 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, CHARGE syndrome
RS2487998678 Health Risk Conflicting classifications of pathogenicity CHD7-related disorder, CHARGE syndrome, CHD7-related disorder
RS2488056894 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia, CHARGE syndrome
RS2488072248 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia, CHARGE syndrome
RS2488143378 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia, CHARGE syndrome
RS267606724 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia
RS34979623 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia, Inborn genetic diseases
RS367615733 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, CHARGE syndrome
RS367722051 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia, CHARGE syndrome
RS367756884 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Inborn genetic diseases, CHARGE syndrome
RS368086966 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, CHARGE syndrome
RS368160678 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Inborn genetic diseases, CHARGE syndrome
RS368609862 Health Risk Conflicting classifications of pathogenicity Hypogonadotropic hypogonadism 5 with or without anosmia, CHARGE syndrome, Inborn genetic diseases
RS368648424 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia, CHD7-related disorder
RS368747227 Health Risk Conflicting classifications of pathogenicity CHARGE syndrome, Hypogonadotropic hypogonadism 5 with or without anosmia, CHD7-related disorder
RS368919638 Health Risk Conflicting classifications of pathogenicity Hypogonadotropic hypogonadism 5 with or without anosmia, CHARGE syndrome, Inborn genetic diseases
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