Variant (rsID / SNP)

rs932061

rs932061 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MMD2. Location: chromosome 7, position 4,959,807. The table records no clinical significance for this variant.

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Reference-table entries

MMD2Not classified

Variant type: synonymous_variant
Chromosome / position: 7:4959807
HGVS: NM_001100600.2,c.285C>T,p.His95His
Allele change: Silent

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.