Variant (rsID / SNP)

rs20556

rs20556 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMB1. Location: chromosome 7, position 107,593,989. 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: 7:107593989
Cytoband: 7q31.1
HGVS: NM_002291.3(LAMB1):c.3065A>G (p.Gln1022Arg)
Allele change: Missense_Q1022R

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.