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rs397515373

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515373(A;A)
Make rs397515373(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position190062219
GeneMSTN
is asnp
is mentioned by
dbSNPrs397515373
ebirs397515373
HLIrs397515373
Exacrs397515373
Varsomers397515373
Maprs397515373
PheGenIrs397515373
hapmaprs397515373
1000 genomesrs397515373
hgdprs397515373
ensemblrs397515373
gopubmedrs397515373
geneviewrs397515373
scholarrs397515373
googlers397515373
pharmgkbrs397515373
gwascentralrs397515373
openSNPrs397515373
23andMers397515373
23andMe allrs397515373
SNP Nexus

SNPshotrs397515373
SNPdbers397515373
MSV3drs397515373
GWAS Ctlgrs397515373
Max Magnitude0
ClinVar
Risk rs397515373(A;A)
Alt rs397515373(A;A)
Reference rs397515373(G;G)
Significance Pathogenic
Disease Muscle hypertrophy
Variation info
Gene C2orf88 MSTN
CLNDBN Muscle hypertrophy
Reversed 1
HGVS NC_000002.11:g.190926945C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008144.2,