Variant (rsID / SNP)

rs149637884

rs149637884 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRRC51, LRTOMT. Location: chromosome 11, position 71,806,057. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

LRRC51Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 11:71806057
Cytoband: 11q13.4
HGVS: NM_145309.6(LRRC51):c.352G>C (p.Gly118Arg)
Allele change: Missense_G118R

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.