rs727502798

Orientation

minus

Stabilized

minus

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

Make rs727502798(-;-)

Make rs727502798(-;ACA)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

69119250

Gene

LMOD3

is a	snp
is	mentioned by
dbSNP	rs727502798
dbSNP (classic)	rs727502798
ClinGen	rs727502798
ebi	rs727502798
HLI	rs727502798
Exac	rs727502798
Gnomad	rs727502798
Varsome	rs727502798
LitVar	rs727502798
Map	rs727502798
PheGenI	rs727502798
Biobank	rs727502798
1000 genomes	rs727502798
hgdp	rs727502798
ensembl	rs727502798
geneview	rs727502798
scholar	rs727502798
google	rs727502798
pharmgkb	rs727502798
gwascentral	rs727502798
openSNP	rs727502798
23andMe	rs727502798
SNPshot	rs727502798
SNPdbe	rs727502798
MSV3d	rs727502798
GWAS Ctlg	rs727502798

Max Magnitude

0

ClinVar
Risk	rs727502798(-;-)
Alt	rs727502798(-;-)
Reference	Rs727502798(ACA;ACA)
Significance	Pathogenic
Disease	Nemaline myopathy 10
Variation	info
Gene	LMOD3
CLNDBN	Nemaline myopathy 10
Reversed	1
HGVS	NC_000003.11:g.69168401_69168403delTGT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000149596.4,