Variant (rsID / SNP)

rs35915664

rs35915664 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMB1. Location: chromosome 7, position 107,569,962. 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: 7:107569962
Cytoband: 7q31.1
HGVS: NM_002291.3(LAMB1):c.4640T>C (p.Ile1547Thr)
Allele change: Missense_I1547T

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.