rs121908961

Orientation

plus

Stabilized

plus

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

Make rs121908961(A;G)

Make rs121908961(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

71667376

Gene

DYSF

is a	snp
is	mentioned by
dbSNP	rs121908961
dbSNP (classic)	rs121908961
ClinGen	rs121908961
ebi	rs121908961
HLI	rs121908961
Exac	rs121908961
Gnomad	rs121908961
Varsome	rs121908961
LitVar	rs121908961
Map	rs121908961
PheGenI	rs121908961
Biobank	rs121908961
1000 genomes	rs121908961
hgdp	rs121908961
ensembl	rs121908961
geneview	rs121908961
scholar	rs121908961
google	rs121908961
pharmgkb	rs121908961
gwascentral	rs121908961
openSNP	rs121908961
23andMe	rs121908961
SNPshot	rs121908961
SNPdbe	rs121908961
MSV3d	rs121908961
GWAS Ctlg	rs121908961

Max Magnitude

0

OMIM	603009
Desc
Variant	0014
Related	also

ClinVar
Risk	rs121908961(G;G)
Alt	rs121908961(G;G)
Reference	Rs121908961(A;A)
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.71894506A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007065.4,