rs387906882

Orientation

plus

Stabilized

plus

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

Make rs387906882(A;A)

Make rs387906882(A;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

137870668

Gene	LOC101928005, MYOT

is a	snp
is	mentioned by
dbSNP	rs387906882
dbSNP (classic)	rs387906882
ClinGen	rs387906882
ebi	rs387906882
HLI	rs387906882
Exac	rs387906882
Gnomad	rs387906882
Varsome	rs387906882
LitVar	rs387906882
Map	rs387906882
PheGenI	rs387906882
Biobank	rs387906882
1000 genomes	rs387906882
hgdp	rs387906882
ensembl	rs387906882
geneview	rs387906882
scholar	rs387906882
google	rs387906882
pharmgkb	rs387906882
gwascentral	rs387906882
openSNP	rs387906882
23andMe	rs387906882
SNPshot	rs387906882
SNPdbe	rs387906882
MSV3d	rs387906882
GWAS Ctlg	rs387906882

Max Magnitude

0

ClinVar
Risk	rs387906882(A;A)
Alt	rs387906882(A;A)
Reference	Rs387906882(G;G)
Significance	Pathogenic
Disease	Limb-girdle muscular dystrophy
Variation	info
Gene	MYOT LOC101928005
CLNDBN	Limb-girdle muscular dystrophy, type 1A
Reversed	0
HGVS	NC_000005.9:g.137206357G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000023360.3,