Variant (rsID / SNP)

rs200302468

rs200302468 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KMT2C. Location: chromosome 7, position 151,860,499. The table records no clinical significance for this variant.

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Reference-table entries

KMT2CNot classified

Variant type: single nucleotide variant
Chromosome / position: 7:151860499
Cytoband: 7q36.1
HGVS: NM_170606.3(KMT2C):c.10163A>G (p.Asn3388Ser)
Allele change: Missense_N3388T

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.