Variant (rsID / SNP)

rs140146478

rs140146478 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMB1. Location: chromosome 7, position 107,626,756. 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: 7:107626756
Cytoband: 7q31.1
HGVS: NM_002291.3(LAMB1):c.476C>G (p.Thr159Ser)
Allele change: Missense_T159S

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.