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Variant (rsID / SNP)

rs79670608

MCM9

rs79670608 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MCM9. Location: chromosome 6, position 119,137,147. The table records no clinical significance for this variant.

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Reference-table entries

MCM9Not classified
Variant type
missense_variant
Chromosome / position
6:119137147
HGVS
NM_001378356.1,c.2272A>G,p.Thr758Ala
Allele change
Missense_T758A

Public references

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