Variant (rsID / SNP)
rs2856111
rs2856111 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC2. Location: chromosome 11, position 1,075,747. The table records no clinical significance for this variant.
Reference-table entries
MUC2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:1075747
- HGVS
- NM_002457.4,c.173T>C,p.Leu58Pro
- Allele change
- Missense_L58P
Associated conditions / phenotypes
Endometriosis|Infertility
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.