GENETIC ENCYCLOPEDIA
ABOUT US    

   

NM_001367624.1(ZNF469):c.1020C>T (p.Gly340=) AND Keratoconus 1

Significance: Benign
ClinVar: RCV000114771

Variant: NM_001367624.1(ZNF469):c.1020C>T (p.Gly340=)

Type: Variant
Allele: NM_001367624.1(ZNF469):c.1020C>T (p.Gly340=) 132428
Gene:
Type: single nucleotide variant
Location: Chr16: 88494898 - assembly GRCh37
Chr16: 88428490 - assembly GRCh38
References: dbSNP: 273585633

Condition

Disease: Keratoconus 1