Variant (rsID / SNP)

rs368800650

rs368800650 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAP2K1. Location: chromosome 15, position 66,782,110. Clinical significance in the table: Likely benign.

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Reference-table entries

MAP2K1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 15:66782110
Cytoband: 15q22.31
HGVS: NM_002755.4(MAP2K1):c.1068+9A>G
Allele change: Silent

Associated conditions / phenotypes

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.