Variant (rsID / SNP)

rs35349706

rs35349706 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRMDA. Location: chromosome 10, position 78,084,184. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LRMDABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:78084184
Cytoband: 10q22.3
HGVS: NM_001305581.2(LRMDA):c.542C>T (p.Ser181Phe)
Allele change: Missense_S181F

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.