Variant (rsID / SNP)

rs113642581

rs113642581 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LYRM7. Location: chromosome 5, position 130,515,811. Clinical significance in the table: Benign.

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Reference-table entries

LYRM7Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:130515811
Cytoband: 5q23.3
HGVS: NM_181705.4(LYRM7):c.42G>A (p.Leu14=)
Allele change: Synonymous_L14L

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.