Variant (rsID / SNP)

rs41289902

rs41289902 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LAMA4. Location: chromosome 6, position 112,460,365. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LAMA4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:112460365
Cytoband: 6q21
HGVS: NM_001105206.3(LAMA4):c.3239G>A (p.Arg1080Gln)
Allele change: Missense_R1080Q

Associated conditions / phenotypes

Dilated cardiomyopathy 1JJ|Cardiomyopathy

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.