Variant (rsID / SNP)

rs11564109

rs11564109 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC19. Location: chromosome 12, position 40,837,898. The table records no clinical significance for this variant.

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Reference-table entries

MUC19Not classified

Variant type: missense_variant
Chromosome / position: 12:40837898
HGVS: NM_173600.2,c.4232G>A,p.Cys1411Tyr
Allele change: Missense_C1411Y

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.