Variant (rsID / SNP)

rs6805421

rs6805421 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KLHL40. Location: chromosome 3, position 42,728,144. Clinical significance in the table: Benign.

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Reference-table entries

KLHL40Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:42728144
Cytoband: 3p22.1
HGVS: NM_152393.4(KLHL40):c.1034A>G (p.Asn345Ser)
Allele change: Missense_N345S

Associated conditions / phenotypes

Nemaline myopathy 8

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.