Variant (rsID / SNP)

rs1895364

rs1895364 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC16. Location: chromosome 19, position 9,057,687. The table records no clinical significance for this variant.

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Reference-table entries

MUC16Not classified

Variant type: missense_variant
Chromosome / position: 19:9057687
HGVS: NM_001401501.1,c.29879T>C,p.Ile9960Thr
Allele change: Missense_I9920T

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.