Variant (rsID / SNP)

rs1805086

rs1805086 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MSTN. Location: chromosome 2, position 190,925,077. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

MSTNBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:190925077
Cytoband: 2q32.2
HGVS: NM_005259.3(MSTN):c.458A>G (p.Lys153Arg)
Allele change: Missense_K153R

Associated conditions / phenotypes

Myostatin-related 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.