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Variant (rsID / SNP)

rs150328852

KMT2A

rs150328852 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KMT2A. Location: chromosome 11, position 118,343,684. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

KMT2AConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:118343684
Cytoband
11q23.3
HGVS
NM_001197104.2(KMT2A):c.1810A>G (p.Met604Val)
Allele change
Missense_M604V

Public references

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