Variant (rsID / SNP)

rs74416301

rs74416301 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HOMER2. Location: chromosome 15, position 83,519,927. Clinical significance in the table: Benign.

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Reference-table entries

HOMER2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:83519927
Cytoband: 15q25.2
HGVS: NM_004839.4(HOMER2):c.819C>T (p.Cys273=)
Allele change: Synonymous_C284C

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.