Variant (rsID / SNP)

rs41273327

rs41273327 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MDN1. Location: chromosome 6, position 90,384,274. 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: 6:90384274
Cytoband: 6q15
HGVS: NM_014611.3(MDN1):c.12796A>G (p.Arg4266Gly)
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.