Variant (rsID / SNP)

rs1801203

rs1801203 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAG1. Location: chromosome 11, position 36,595,321. Clinical significance in the table: Benign.

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Reference-table entries

RAG1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:36595321
Cytoband: 11p12
HGVS: NM_000448.3(RAG1):c.467C>T (p.Ala156Val)
Allele change: Missense_A156V

Associated conditions / phenotypes

RECOMBINATION ACTIVATING GENE 1 POLYMORPHISM

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.