Variant (rsID / SNP)

rs115518856

rs115518856 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMB1. Location: chromosome 7, position 107,603,471. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

LAMB1Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 7:107603471
Cytoband: 7q31.1
HGVS: NM_002291.3(LAMB1):c.1736G>A (p.Arg579Gln)
Allele change: Missense_R579Q

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.