Variant (rsID / SNP)

rs10901344

rs10901344 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMC3. Location: chromosome 9, position 133,946,909. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LAMC3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 9:133946909
Cytoband: 9q34.12
HGVS: NM_006059.4(LAMC3):c.3108G>A (p.Gly1036=)
Allele change: Synonymous_G1036G

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.