rs121908461

Orientation

plus

Stabilized

plus

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

Make rs121908461(C;T)

Make rs121908461(T;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

137870767

Gene	LOC101928005, MYOT

is a	snp
is	mentioned by
dbSNP	rs121908461
dbSNP (classic)	rs121908461
ClinGen	rs121908461
ebi	rs121908461
HLI	rs121908461
Exac	rs121908461
Gnomad	rs121908461
Varsome	rs121908461
LitVar	rs121908461
Map	rs121908461
PheGenI	rs121908461
Biobank	rs121908461
1000 genomes	rs121908461
hgdp	rs121908461
ensembl	rs121908461
geneview	rs121908461
scholar	rs121908461
google	rs121908461
pharmgkb	rs121908461
gwascentral	rs121908461
openSNP	rs121908461
23andMe	rs121908461
SNPshot	rs121908461
SNPdbe	rs121908461
MSV3d	rs121908461
GWAS Ctlg	rs121908461

Max Magnitude

0

OMIM	604103
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121908461(T;T)
Alt	rs121908461(T;T)
Reference	Rs121908461(C;C)
Significance	Pathogenic
Disease	Spheroid body myopathy
Variation	info
Gene	MYOT LOC101928005
CLNDBN	Spheroid body myopathy
Reversed	0
HGVS	NC_000005.9:g.137206456C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006196.3,