Variant (rsID / SNP)

rs11168830

rs11168830 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KMT2D. Location: chromosome 12, position 49,424,534. Clinical significance in the table: Benign.

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Reference-table entries

KMT2DBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:49424534
Cytoband: 12q13.12
HGVS: NM_003482.4(KMT2D):c.13689C>T (p.Pro4563=)
Allele change: Synonymous_P4563P

Associated conditions / phenotypes

Kabuki syndrome

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.