Variant (rsID / SNP)

rs201609456

rs201609456 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMB1. Location: chromosome 7, position 107,569,959. Clinical significance in the table: Uncertain significance.

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Reference-table entries

LAMB1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 7:107569959
Cytoband: 7q31.1
HGVS: NM_002291.3(LAMB1):c.4643G>A (p.Arg1548His)
Allele change: Missense_R1548H

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.