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Variant (rsID / SNP)

rs727504424

HRAS

rs727504424 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HRAS. Location: chromosome 11, position 534,287. The table records no clinical significance for this variant.

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Reference-table entries

HRASNot classified
Variant type
single nucleotide variant
Chromosome / position
11:534287
Cytoband
11p15.5
HGVS
NM_005343.4(HRAS):c.36C>A (p.Gly12=)
Allele change
Synonymous_G12G

Public references

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