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Variant (rsID / SNP)

rs150170255

DNM1L

rs150170255 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNM1L. Location: chromosome 12, position 32,863,908. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

DNM1LConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
12:32863908
Cytoband
12p11.21
HGVS
NM_012062.5(DNM1L):c.415G>A (p.Val139Ile)
Allele change
Missense_V139I

Public references

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