Variant (rsID / SNP)

rs2158935

rs2158935 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CACTIN. Location: chromosome 19, position 3,611,972. The table records no clinical significance for this variant.

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Reference-table entries

CACTINNot classified

Variant type: synonymous_variant
Chromosome / position: 19:3611972
HGVS: NM_001080543.2,c.2226C>T,p.Asn742Asn
Allele change: Silent

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.