Variant (rsID / SNP)

rs20555

rs20555 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMB1. Location: chromosome 7, position 107,601,751. Clinical significance in the table: Benign.

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Reference-table entries

LAMB1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:107601751
Cytoband: 7q31.1
HGVS: NM_002291.3(LAMB1):c.2009T>C (p.Val670Ala)
Allele change: Missense_V670A

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.