Variant (rsID / SNP)

rs4252633

rs4252633 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ERBB2. Location: chromosome 17, position 37,872,035. Clinical significance in the table: Benign.

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Reference-table entries

ERBB2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:37872035
Cytoband: 17q12
HGVS: NM_004448.4(ERBB2):c.1356G>T (p.Trp452Cys)
Allele change: Missense_W422C

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.