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Variant (rsID / SNP)

rs602990

VAV2

rs602990 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VAV2. Location: chromosome 9, position 136,643,994. The table records no clinical significance for this variant.

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Reference-table entries

VAV2Not classified
Variant type
missense_variant
Chromosome / position
9:136643994
HGVS
NM_001134398.2,c.1780A>G,p.Met594Val
Allele change
Missense_M594V

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.