Variant (rsID / SNP)

rs76776920

rs76776920 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NALCN. Location: chromosome 13, position 101,763,029. Clinical significance in the table: Benign.

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Reference-table entries

NALCNBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 13:101763029
Cytoband: 13q33.1
HGVS: NM_052867.4(NALCN):c.2305C>T (p.His769Tyr)
Allele change: Missense_H740Y

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.