Variant (rsID / SNP)

rs142739534

rs142739534 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NRAS. Location: chromosome 1, position 115,256,486. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

NRASBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:115256486
Cytoband: 1p13.2
HGVS: NM_002524.5(NRAS):c.225C>T (p.Gly75=)
Allele change: Synonymous_G75G

Associated conditions / phenotypes

Noonan syndrome 6|RASopathy

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.