Variant (rsID / SNP)

rs7245949

rs7245949 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC16. Location: chromosome 19, position 9,083,143. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MUC16Not classified

Variant type: missense_variant
Chromosome / position: 19:9083143
HGVS: NM_001401501.1,c.8792C>T,p.Thr2931Ile
Allele change: Missense_T2891I

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.