Variant (rsID / SNP)

rs117509372

rs117509372 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VAV1. Location: chromosome 19, position 6,833,210. Clinical significance in the table: Benign.

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Reference-table entries

VAV1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:6833210
Cytoband: 19p13.3
HGVS: NM_005428.4(VAV1):c.1524G>A (p.Pro508=)
Allele change: Synonymous_P508P

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.