Variant (rsID / SNP)

rs16882046

rs16882046 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MDN1. Location: chromosome 6, position 90,374,283. Clinical significance in the table: Benign.

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Reference-table entries

MDN1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:90374283
Cytoband: 6q15
HGVS: NM_014611.3(MDN1):c.14159T>C (p.Ile4720Thr)
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.