rs104893868

Orientation

minus

Stabilized

minus

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

Make rs104893868(G;G)

Make rs104893868(G;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

52028799

Gene

SGCB

is a	snp
is	mentioned by
dbSNP	rs104893868
dbSNP (classic)	rs104893868
ClinGen	rs104893868
ebi	rs104893868
HLI	rs104893868
Exac	rs104893868
Gnomad	rs104893868
Varsome	rs104893868
LitVar	rs104893868
Map	rs104893868
PheGenI	rs104893868
Biobank	rs104893868
1000 genomes	rs104893868
hgdp	rs104893868
ensembl	rs104893868
geneview	rs104893868
scholar	rs104893868
google	rs104893868
pharmgkb	rs104893868
gwascentral	rs104893868
openSNP	rs104893868
23andMe	rs104893868
SNPshot	rs104893868
SNPdbe	rs104893868
MSV3d	rs104893868
GWAS Ctlg	rs104893868

Max Magnitude

0

OMIM	600900
Desc
Variant	0002
Related	also

ClinVar
Risk	rs104893868(G;G)
Alt	rs104893868(G;G)
Reference	Rs104893868(T;T)
Significance	Other
Disease	Limb-girdle muscular dystrophy
Variation	info
Gene	SGCB
CLNDBN	Limb-girdle muscular dystrophy, type 2E
Reversed	1
HGVS	NC_000004.11:g.52894965A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009251.3,