Variant (rsID / SNP)

rs56219475

rs56219475 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SOS1. Location: chromosome 2, position 39,241,107. Clinical significance in the table: Benign.

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Reference-table entries

SOS1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:39241107
Cytoband: 2p22.1
HGVS: NM_005633.4(SOS1):c.1964C>T (p.Pro655Leu)
Allele change: Missense_P655L

Associated conditions / phenotypes

RASopathy|Arrhythmogenic right ventricular cardiomyopathy|Noonan syndrome 4|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.