Variant (rsID / SNP)

rs377675706

rs377675706 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAP2K2. Location: chromosome 19, position 4,090,588. Clinical significance in the table: Likely benign.

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Reference-table entries

MAP2K2Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 19:4090588
Cytoband: 19p13.3
HGVS: NM_030662.3(MAP2K2):c.*8C>T
Allele change: Silent

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.