Variant (rsID / SNP)

rs236110

rs236110 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MCM8, TRMT6. Location: chromosome 20, position 5,933,108. The table records no clinical significance for this variant.

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Reference-table entries

MCM8Not classified

Variant type: missense_variant
Chromosome / position: 20:5933108
HGVS: NM_001281521.2,c.187C>A,p.Gln63Lys
Allele change: Missense_Q63K

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.