rs121434447

Orientation

plus

Stabilized

plus

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

Make rs121434447(A;A)

Make rs121434447(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

116698923

Gene	ASTN2, TRIM32

is a	snp
is	mentioned by
dbSNP	rs121434447
dbSNP (classic)	rs121434447
ClinGen	rs121434447
ebi	rs121434447
HLI	rs121434447
Exac	rs121434447
Gnomad	rs121434447
Varsome	rs121434447
LitVar	rs121434447
Map	rs121434447
PheGenI	rs121434447
Biobank	rs121434447
1000 genomes	rs121434447
hgdp	rs121434447
ensembl	rs121434447
geneview	rs121434447
scholar	rs121434447
google	rs121434447
pharmgkb	rs121434447
gwascentral	rs121434447
openSNP	rs121434447
23andMe	rs121434447
SNPshot	rs121434447
SNPdbe	rs121434447
MSV3d	rs121434447
GWAS Ctlg	rs121434447

Max Magnitude

0

OMIM	602290
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121434447(A;A)
Alt	rs121434447(A;A)
Reference	Rs121434447(G;G)
Significance	Pathogenic
Disease	Sarcotubular myopathy not specified
Variation	info
Gene	TRIM32 ASTN2
CLNDBN	Sarcotubular myopathy not specified
Reversed	0
HGVS	NC_000009.11:g.119461202G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007778.3, RCV000362326.1,