rs724159965

Orientation

minus

Stabilized

minus

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

Make rs724159965(G;T)

Make rs724159965(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

69119286

Gene

LMOD3

is a	snp
is	mentioned by
dbSNP	rs724159965
dbSNP (classic)	rs724159965
ClinGen	rs724159965
ebi	rs724159965
HLI	rs724159965
Exac	rs724159965
Gnomad	rs724159965
Varsome	rs724159965
LitVar	rs724159965
Map	rs724159965
PheGenI	rs724159965
Biobank	rs724159965
1000 genomes	rs724159965
hgdp	rs724159965
ensembl	rs724159965
geneview	rs724159965
scholar	rs724159965
google	rs724159965
pharmgkb	rs724159965
gwascentral	rs724159965
openSNP	rs724159965
23andMe	rs724159965
SNPshot	rs724159965
SNPdbe	rs724159965
MSV3d	rs724159965
GWAS Ctlg	rs724159965

Max Magnitude

0

ClinVar
Risk	rs724159965(T;T)
Alt	rs724159965(T;T)
Reference	Rs724159965(G;G)
Significance	Pathogenic
Disease	Nemaline myopathy 10
Variation	info
Gene	LMOD3
CLNDBN	Nemaline myopathy 10
Reversed	1
HGVS	NC_000003.11:g.69168437C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000149599.4,