Variant (rsID / SNP)

rs10761581

rs10761581 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NCOA4. Location: chromosome 10, position 51,568,378. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

NCOA4Not classified

Variant type: missense_variant
Chromosome / position: 10:51568378
HGVS: NM_001145260.2,c.22T>G,p.Phe8Val
Allele change: Silent

Associated conditions / phenotypes

Myopathy, Myosin Storage, Autosomal Recessive|Skin Carcinoma

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.