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Variant (rsID / SNP)

rs35883486

CAVIN2

rs35883486 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAVIN2. Location: chromosome 2, position 192,711,385. The table records no clinical significance for this variant.

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Reference-table entries

CAVIN2Not classified
Variant type
synonymous_variant
Chromosome / position
2:192711385
HGVS
NM_004657.6,c.267C>T,p.Ser89Ser
Allele change
Synonymous_S89S

Public references

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