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Variant (rsID / SNP)

rs121917759

HRAS

rs121917759 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HRAS. Location: chromosome 11, position 533,466. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

HRASLikely pathogenic
Clinical significance (as recorded)
Likely pathogenic
Variant type
single nucleotide variant
Chromosome / position
11:533466
Cytoband
11p15.5
HGVS
NM_005343.4(HRAS):c.437C>T (p.Ala146Val)
Allele change
Missense_A146V

Associated conditions / phenotypes

Costello syndrome|Neoplasm of the large intestine|Gastric adenocarcinoma|Multiple myeloma|Acute myeloid leukemia|Neoplasm of uterine cervix|Lung adenocarcinoma

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.