rs121908960

Orientation

plus

Stabilized

plus

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

Make rs121908960(G;T)

Make rs121908960(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

71553131

Gene

DYSF

is a	snp
is	mentioned by
dbSNP	rs121908960
dbSNP (classic)	rs121908960
ClinGen	rs121908960
ebi	rs121908960
HLI	rs121908960
Exac	rs121908960
Gnomad	rs121908960
Varsome	rs121908960
LitVar	rs121908960
Map	rs121908960
PheGenI	rs121908960
Biobank	rs121908960
1000 genomes	rs121908960
hgdp	rs121908960
ensembl	rs121908960
geneview	rs121908960
scholar	rs121908960
google	rs121908960
pharmgkb	rs121908960
gwascentral	rs121908960
openSNP	rs121908960
23andMe	rs121908960
SNPshot	rs121908960
SNPdbe	rs121908960
MSV3d	rs121908960
GWAS Ctlg	rs121908960

Max Magnitude

0

OMIM	603009
Desc
Variant	0013
Related	also

ClinVar
Risk	rs121908960(A;A) rs121908960(T;T)
Alt	rs121908960(A;A) rs121908960(T;T)
Reference	Rs121908960(G;G)
Significance	Pathogenic
Disease	Limb-girdle muscular dystrophy
Variation	info
Gene	DYSF
CLNDBN	Limb-girdle muscular dystrophy, type 2B
Reversed	0
HGVS	NC_000002.11:g.71780261G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007064.5,