Variant (rsID / SNP)

rs140919432

rs140919432 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KMT2C. Location: chromosome 7, position 151,949,698. Clinical significance in the table: Likely benign.

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Reference-table entries

KMT2CLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 7:151949698
Cytoband: 7q36.1
HGVS: NM_170606.3(KMT2C):c.1402C>A (p.Pro468Thr)
Allele change: Missense_P468T

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.