Variant (rsID / SNP)

rs10901333

rs10901333 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMC3. Location: chromosome 9, position 133,927,878. 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: 9:133927878
Cytoband: 9q34.12
HGVS: NM_006059.4(LAMC3):c.1631A>G (p.Glu544Gly)
Allele change: Missense_E544G

Associated conditions / phenotypes

Occipital pachygyria and polymicrogyria

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.