GENETIC ENCYCLOPEDIA
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NM_001367624.1(ZNF469):c.10573G>A (p.Glu3525Lys) AND Keratoconus 1

Significance: Benign
ClinVar: RCV000114772

Variant: NM_001367624.1(ZNF469):c.10573G>A (p.Glu3525Lys)

Type: Variant
Allele: NM_001367624.1(ZNF469):c.10573G>A (p.Glu3525Lys) 132429
Gene:
Type: single nucleotide variant
Location: Chr16: 88504451 - assembly GRCh37
Chr16: 88438043 - assembly GRCh38
References: dbSNP: 273585628

Condition

Disease: Keratoconus 1