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Variant (rsID / SNP)

rs2291652

MUC4

rs2291652 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC4. Location: chromosome 3, position 195,477,791. The table records no clinical significance for this variant.

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Reference-table entries

MUC4Not classified
Variant type
synonymous_variant
Chromosome / position
3:195477791
HGVS
NM_018406.7,c.15840C>T,p.Ile5280Ile
Allele change
Missense_S4542F

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.