Variant (rsID / SNP)

rs295322

rs295322 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RASA2. Location: chromosome 3, position 141,326,602. Clinical significance in the table: Benign.

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Reference-table entries

RASA2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:141326602
Cytoband: 3q23
HGVS: NM_006506.5(RASA2):c.2016T>C (p.Asn672=)
Allele change: Synonymous_N673N

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.