Variant (rsID / SNP)

rs763337946

rs763337946 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SOS1. Location: chromosome 2, position 39,347,525. Clinical significance in the table: Likely benign.

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Reference-table entries

SOS1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 2:39347525
Cytoband: 2p22.1
HGVS: NM_005633.4(SOS1):c.39A>G (p.Glu13=)
Allele change: Synonymous_E13E

Associated conditions / phenotypes

RASopathy|Noonan syndrome and Noonan-related 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.