Variant (rsID / SNP)

rs1609459

rs1609459 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC16. Location: chromosome 19, position 9,084,216. The table records no clinical significance for this variant.

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Reference-table entries

MUC16Not classified

Variant type: synonymous_variant
Chromosome / position: 19:9084216
HGVS: NM_001401501.1,c.7719A>G,p.Ala2573Ala
Allele change: Synonymous_A2533A

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.