rs121908335

Orientation

plus

Stabilized

plus

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

Make rs121908335(C;T)

Make rs121908335(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

86699324

Gene

LDB3

is a	snp
is	mentioned by
dbSNP	rs121908335
dbSNP (classic)	rs121908335
ClinGen	rs121908335
ebi	rs121908335
HLI	rs121908335
Exac	rs121908335
Gnomad	rs121908335
Varsome	rs121908335
LitVar	rs121908335
Map	rs121908335
PheGenI	rs121908335
Biobank	rs121908335
1000 genomes	rs121908335
hgdp	rs121908335
ensembl	rs121908335
geneview	rs121908335
scholar	rs121908335
google	rs121908335
pharmgkb	rs121908335
gwascentral	rs121908335
openSNP	rs121908335
23andMe	rs121908335
SNPshot	rs121908335
SNPdbe	rs121908335
MSV3d	rs121908335
GWAS Ctlg	rs121908335

Max Magnitude

0

OMIM	605906
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121908335(T;T)
Alt	rs121908335(T;T)
Reference	Rs121908335(C;C)
Significance	Pathogenic
Disease	Myofibrillar myopathy not specified
Variation	info
Gene	LDB3
CLNDBN	Myofibrillar myopathy, ZASP-related not specified
Reversed	0
HGVS	NC_000010.10:g.88459081C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004994.3, RCV000154745.1,