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Variant (rsID / SNP)

rs11205303

MTMR11

rs11205303 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTMR11. Location: chromosome 1, position 149,906,413. The table records no clinical significance for this variant.

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Reference-table entries

MTMR11Not classified
Variant type
missense_variant
Chromosome / position
1:149906413
HGVS
NM_001145862.2,c.475A>G,p.Met159Val
Allele change
Missense_M87V

Associated conditions / phenotypes

Mammographic Density

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.