Variant (rsID / SNP)

rs150553818

rs150553818 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NECTIN1. Location: chromosome 11, position 119,545,884. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

NECTIN1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 11:119545884
Cytoband: 11q23.3
HGVS: NM_002855.5(NECTIN1):c.988G>A (p.Glu330Lys)
Allele change: Missense_E330K

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.