Variant (rsID / SNP)

rs9444701

rs9444701 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MDN1. Location: chromosome 6, position 90,371,202. The table records no clinical significance for this variant.

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Reference-table entries

MDN1Not classified

Variant type: synonymous_variant
Chromosome / position: 6:90371202
HGVS: NM_014611.3,c.14661C>T,p.Leu4887Leu
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.