H3-3A, H3.3 histone A, 3020

N. diseases: 134; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C0028738
Disease:
Nystagmus 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C0024636
Disease:
Malocclusion 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C1865186
Disease:
Bell-shaped thorax 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C0700292
Disease:
Hypoxemia 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C0019209
Disease:
Hepatomegaly 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C1837404
Disease:
High, narrow palate 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C0265865
Disease:
Mesocardia 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C1844820
Disease:
Range of joint movement increased 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C4023343
Disease:
Nasogastric tube feeding in infancy 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C4021467
Disease:
Contracture of the proximal interphalangeal joint of the 3rd finger 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C0039231
Disease:
Tachycardia 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C1842364
Disease:
Central hypotonia 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C4024170
Disease:
Localized hirsutism 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C0221358
Disease:
Long narrow head 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C0557874
Disease:
Global developmental delay 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C0006157
Disease:
Breech Presentation 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C0038379
Disease:
Strabismus 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C0221766
Disease:
Diastasis recti 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C4048268
Disease:
Cortical visual impairment 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C1857949
Disease:
Prominent metopic ridge 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C0020534
Disease:
Orbital separation excessive 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C0264303
Disease:
Laryngomalacia 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C0948187
Disease:
Tracheomalacia 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C0042798
Disease:
Low Vision 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1276519904
rs1276519904
Entrez Id: 3020
Gene Symbol: H3-3A
H3-3A
CUI: C0221354
Disease:
Frontal bossing 		G 0.700 GeneticVariation CLINVAR