Variant (rsID / SNP)

rs60106152

rs60106152 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC16. Location: chromosome 19, position 9,083,791. The table records no clinical significance for this variant.

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Reference-table entries

MUC16Not classified

Variant type: missense_variant
Chromosome / position: 19:9083791
HGVS: NM_001401501.1,c.8144C>T,p.Ser2715Leu
Allele change: Missense_S2675L

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.