Variant (rsID / SNP)

rs41317471

rs41317471 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HMCN1. Location: chromosome 1, position 185,976,370. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

HMCN1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:185976370
Cytoband: 1q31.1
HGVS: NM_031935.3(HMCN1):c.4586A>G (p.Asn1529Ser)
Allele change: Missense_N1529S

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.