HVCN1, hydrogen voltage gated channel 1, 84329

N. diseases: 16; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs534772444
rs534772444
Entrez Id: 84329
Gene Symbol: HVCN1
HVCN1
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs751962801
rs751962801
Entrez Id: 79600;84329
Gene Symbol: TCTN1;HVCN1
TCTN1;HVCN1
CUI: C3280031
Disease:
JOUBERT SYNDROME 13 		T 0.700 CausalMutation CLINVAR
dbSNP: rs797046039
rs797046039
Entrez Id: 79600;84329
Gene Symbol: TCTN1;HVCN1
TCTN1;HVCN1
CUI: C3280031
Disease:
JOUBERT SYNDROME 13 		A 0.700 CausalMutation CLINVAR