Variant (rsID / SNP)

rs61741195

rs61741195 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRTOMT, ANAPC15. Location: chromosome 11, position 71,819,718. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LRTOMTBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:71819718
Cytoband: 11q13.4
HGVS: NM_001393500.2(TOMT):c.524G>A (p.Arg175Gln)
Allele change: Missense_R208Q

Associated conditions / phenotypes

Autosomal recessive nonsyndromic hearing loss 63

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.