Variant (rsID / SNP)

rs6693069

rs6693069 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HMCN1. Location: chromosome 1, position 186,113,727. Clinical significance in the table: Benign.

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Reference-table entries

HMCN1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:186113727
Cytoband: 1q31.1
HGVS: NM_031935.3(HMCN1):c.14158G>A (p.Ala4720Thr)
Allele change: Missense_A4720T

Associated conditions / phenotypes

Age related macular degeneration 1

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.