rs397515373

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs397515373(A;A)

Make rs397515373(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

190062219

Gene	C2orf88, MSTN

is a	snp
is	mentioned by
dbSNP	rs397515373
dbSNP (classic)	rs397515373
ClinGen	rs397515373
ebi	rs397515373
HLI	rs397515373
Exac	rs397515373
Gnomad	rs397515373
Varsome	rs397515373
LitVar	rs397515373
Map	rs397515373
PheGenI	rs397515373
Biobank	rs397515373
1000 genomes	rs397515373
hgdp	rs397515373
ensembl	rs397515373
geneview	rs397515373
scholar	rs397515373
google	rs397515373
pharmgkb	rs397515373
gwascentral	rs397515373
openSNP	rs397515373
23andMe	rs397515373
SNPshot	rs397515373
SNPdbe	rs397515373
MSV3d	rs397515373
GWAS Ctlg	rs397515373

Max Magnitude

0

ClinVar
Risk	rs397515373(A;A)
Alt	rs397515373(A;A)
Reference	Rs397515373(G;G)
Significance	Pathogenic
Disease	Muscle hypertrophy
Variation	info
Gene	MSTN C2orf88
CLNDBN	Muscle hypertrophy
Reversed	1
HGVS	NC_000002.11:g.190926945C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008144.2,