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
RS367557471 Health Risk Likely pathogenic Atrial septal defect, Pyloric stenosis, Abnormal facial shape
RS587783432 Health Risk Likely pathogenic CHARGE syndrome, Inborn genetic diseases, CHARGE syndrome
RS587783441 Health Risk Likely pathogenic CHARGE syndrome, CHARGE syndrome
RS587783445 Health Risk Likely pathogenic CHARGE syndrome, CHARGE syndrome
RS755066542 Health Risk Likely pathogenic CHARGE syndrome, CHARGE syndrome
RS769587871 Health Risk Likely pathogenic
RS770166812 Health Risk Likely pathogenic CHARGE syndrome, CHARGE syndrome
RS773138428 Health Risk Likely pathogenic CHARGE syndrome, CHARGE syndrome
RS886039881 Health Risk Likely pathogenic Hypogonadotropic hypogonadism 5 with or without anosmia, Hypogonadotropic hypogonadism 5 with or without anosmia
RS985812567 Health Risk Likely pathogenic CHARGE syndrome, CHARGE syndrome
RS1057517713 Health Risk Pathogenic
RS1057517956 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS1057517957 Health Risk Pathogenic
RS1057518576 Health Risk Pathogenic
RS1057518891 Health Risk Pathogenic 6 conditions, 6 conditions
RS1057519423 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS1057520712 Health Risk Pathogenic
RS1057520734 Health Risk Pathogenic
RS1057524501 Health Risk Pathogenic
RS1060499560 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS1060503180 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS1060503181 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS1060503182 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS1060503184 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS1060503185 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS1060503187 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS1064793346 Health Risk Pathogenic CHARGE syndrome, CHD7-related disorder, CHARGE syndrome
RS1064793432 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS1064793463 Health Risk Pathogenic
RS1064793664 Health Risk Pathogenic
RS1064793769 Health Risk Pathogenic
RS1064793909 Health Risk Pathogenic
RS1064793962 Health Risk Pathogenic
RS1064793972 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS1064793994 Health Risk Pathogenic
RS1064793996 Health Risk Pathogenic
RS1064794040 Health Risk Pathogenic
RS1064794248 Health Risk Pathogenic
RS1085307830 Health Risk Pathogenic
RS1131690787 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS1131691420 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS1131691733 Health Risk Pathogenic
RS1131691892 Health Risk Pathogenic
RS1131692153 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS1131692325 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS121434339 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS121434340 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS121434341 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome, CHD7-related disorder
RS121434342 Health Risk Pathogenic CHARGE syndrome, CHARGE syndrome
RS121434344 Health Risk Pathogenic CHARGE syndrome, HYPOGONADOTROPIC HYPOGONADISM 5 WITHOUT ANOSMIA, CHARGE syndrome
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