Variant (rsID / SNP)

rs117361076

rs117361076 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMC3. Location: chromosome 9, position 133,967,007. Clinical significance in the table: Benign.

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Reference-table entries

LAMC3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 9:133967007
Cytoband: 9q34.12
HGVS: NM_006059.4(LAMC3):c.4561T>G (p.Ser1521Ala)
Allele change: Missense_S1521A

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.