Variant (rsID / SNP)

rs373169526

rs373169526 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRAS. Location: chromosome 12, position 25,368,405. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

KRASConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 12:25368405
Cytoband: 12p12.1
HGVS: NM_004985.5(KRAS):c.451-5560T>A
Allele change: Nonsense_C180X

Associated conditions / phenotypes

Cardio-facio-cutaneous syndrome

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.