Variant (rsID / SNP)

rs61763587

rs61763587 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRAS. Location: chromosome 12, position 25,363,085. Clinical significance in the table: Likely benign.

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Reference-table entries

KRASLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 12:25363085
Cytoband: 12p12.1
HGVS: NM_033360.4(KRAS):c.5-240G>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.