Variant (rsID / SNP)

rs199535979

rs199535979 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMC3. Location: chromosome 9, position 133,945,051. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

LAMC3Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 9:133945051
Cytoband: 9q34.12
HGVS: NM_006059.4(LAMC3):c.2891-8C>T
Allele change: Silent

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.