Variant (rsID / SNP)

rs176026

rs176026 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAGEC3. The table records no clinical significance for this variant.

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Reference-table entries

MAGEC3Not classified

Variant type: missense_variant
HGVS: NM_138702.1,c.982G>A,p.Ala328Thr
Allele change: Missense_A328T

Associated conditions / phenotypes

Ovarian Cancer|Familial Ovarian Cancer

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.