Variant (rsID / SNP)

rs2296262

rs2296262 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WHRN. Location: chromosome 9, position 117,265,406. Clinical significance in the table: Benign.

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Reference-table entries

WHRNBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 9:117265406
Cytoband: 9q32
HGVS: NM_015404.4(WHRN):c.618+1058G>A
Allele change: Silent

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.