Variant (rsID / SNP)

rs4408643

rs4408643 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC16. Location: chromosome 19, position 9,096,252. The table records no clinical significance for this variant.

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Reference-table entries

MUC16Not classified

Variant type: synonymous_variant
Chromosome / position: 19:9096252
HGVS: NM_001401501.1,c.276A>G,p.Val92Val

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.