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rs35781413

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs35781413(A;A)
Make rs35781413(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position190060319
GeneC2orf88, MSTN
is asnp
is mentioned by
dbSNPrs35781413
dbSNP (classic)rs35781413
ClinGenrs35781413
ebirs35781413
HLIrs35781413
Exacrs35781413
Gnomadrs35781413
Varsomers35781413
LitVarrs35781413
Maprs35781413
PheGenIrs35781413
Biobankrs35781413
1000 genomesrs35781413
hgdprs35781413
ensemblrs35781413
geneviewrs35781413
scholarrs35781413
googlers35781413
pharmgkbrs35781413
gwascentralrs35781413
openSNPrs35781413
23andMers35781413
SNPshotrs35781413
SNPdbers35781413
MSV3drs35781413
GWAS Ctlgrs35781413
GMAF0.008264
Max Magnitude0

[PMID 21283721OA-icon.png] The K153R Polymorphism in the Myostatin Gene and Muscle Power Phenotypes in Young, Non-Athletic Men

[PMID 22209717] Association of myostatin gene polymorphisms with obesity in Chinese north Han human subjects [PMID 23354683OA-icon.png] Association of the K153R polymorphism in the myostatin gene and extreme longevity.

ClinVar
Risk rs35781413(A;A)
Alt rs35781413(A;A)
Reference Rs35781413(G;G)
Significance Probable-non-pathogenic
Disease Myostatin-related muscle hypertrophy
Variation info
Gene C2orf88 MSTN
CLNDBN Myostatin-related muscle hypertrophy
Reversed 1
HGVS NC_000002.11:g.190925045C>T
CLNSRC
CLNACC RCV000376122.1,