Variant (rsID / SNP)

rs28750165

rs28750165 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMB1. Location: chromosome 7, position 107,616,188. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LAMB1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:107616188
Cytoband: 7q31.1
HGVS: NM_002291.3(LAMB1):c.1135C>T (p.Pro379Ser)
Allele change: Missense_P379S

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.