Variant (rsID / SNP)

rs146123023

rs146123023 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRMDA. Location: chromosome 10, position 77,542,754. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

LRMDAConflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: Deletion
Chromosome / position: 10:77542754
Cytoband: 10q22.2
HGVS: NM_001305581.2(LRMDA):c.132-253012del

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.