Variant (rsID / SNP)

rs4822783

rs4822783 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LZTR1. Location: chromosome 22, position 21,342,811. Clinical significance in the table: Benign.

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Reference-table entries

LZTR1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 22:21342811
Cytoband: 22q11.21
HGVS: NM_006767.4(LZTR1):c.510-267C>T
Allele change: Silent

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.