Variant (rsID / SNP)

rs76438938

rs76438938 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KNG1. Location: chromosome 3, position 186,461,524. Clinical significance in the table: Benign.

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Reference-table entries

KNG1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:186461524
Cytoband: 3q27.3
HGVS: NM_001102416.3(KNG1):c.*1404C>T
Allele change: Nonsense_R376X

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.