Variant (rsID / SNP)

rs116880118

rs116880118 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MCMDC2. Location: chromosome 8, position 67,789,706. The table records no clinical significance for this variant.

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Reference-table entries

MCMDC2Not classified

Variant type: synonymous_variant
Chromosome / position: 8:67789706
HGVS: NM_173518.5,c.408A>C,p.Ala136Ala
Allele change: Synonymous_A136A

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.