Variant (rsID / SNP)

rs61761625

rs61761625 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WRN. Location: chromosome 8, position 30,922,521. Clinical significance in the table: Uncertain significance.

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Reference-table entries

WRNUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 8:30922521
Cytoband: 8p12
HGVS: NM_000553.6(WRN):c.446G>A (p.Arg149His)
Allele change: Missense_R149H

Associated conditions / phenotypes

Werner syndrome

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.