Variant (rsID / SNP)

rs150804738

rs150804738 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KMT2A. Location: chromosome 11, position 118,375,998. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

KMT2ABenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 11:118375998
Cytoband: 11q23.3
HGVS: NM_001197104.2(KMT2A):c.9391G>A (p.Gly3131Ser)
Allele change: Missense_G3131S

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.