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Variant (rsID / SNP)

rs2246901

MUC4

rs2246901 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MUC4. Location: chromosome 3, position 195,489,009. The table records no clinical significance for this variant.

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Reference-table entries

MUC4Not classified
Variant type
missense_variant
Chromosome / position
3:195489009
HGVS
NM_018406.7,c.14461G>T,p.Ala4821Ser
Allele change
Synonymous_T4082T

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.