Variant (rsID / SNP)

rs104894361

rs104894361 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KRAS. Location: chromosome 12, position 25,398,304. Clinical significance in the table: Pathogenic.

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Reference-table entries

KRASPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 12:25398304
Cytoband: 12p12.1
HGVS: NM_033360.4(KRAS):c.15A>T (p.Lys5Asn)
Allele change: Missense_K5N

Associated conditions / phenotypes

Cardiofaciocutaneous syndrome 2|Noonan syndrome|Inborn genetic diseases

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.