Variant (rsID / SNP)

rs2292462

rs2292462 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR73, NMB. Location: chromosome 15, position 85,200,754. The table records no clinical significance for this variant.

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Reference-table entries

WDR73Not classified

Variant type: upstream_gene_variant
Chromosome / position: 15:85200754
HGVS: NM_032856.5,c.-3249C>A
Allele change: Silent

Associated conditions / phenotypes

Muscle Hypertrophy

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.