rs886044688

Orientation

plus

Stabilized

plus

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

Chromosome

17

Position

50167607

Gene	LOC105371818, SGCA

is a	snp
is	mentioned by
dbSNP	rs886044688
dbSNP (classic)	rs886044688
ClinGen	rs886044688
ebi	rs886044688
HLI	rs886044688
Exac	rs886044688
Gnomad	rs886044688
Varsome	rs886044688
LitVar	rs886044688
Map	rs886044688
PheGenI	rs886044688
Biobank	rs886044688
1000 genomes	rs886044688
hgdp	rs886044688
ensembl	rs886044688
geneview	rs886044688
scholar	rs886044688
google	rs886044688
pharmgkb	rs886044688
gwascentral	rs886044688
openSNP	rs886044688
23andMe	rs886044688
SNPshot	rs886044688
SNPdbe	rs886044688
MSV3d	rs886044688
GWAS Ctlg	rs886044688

Max Magnitude

0

ClinVar
Risk	rs886044688(C;C)
Alt	rs886044688(C;C)
Reference	Rs886044688(-;-)
Significance	Pathogenic
Disease	Limb-girdle muscular dystrophy
Variation	info
Gene	SGCA
CLNDBN	Limb-girdle muscular dystrophy, type 2D
Reversed	0
HGVS	NC_000017.10:g.48244968dupC
CLNSRC
CLNACC	RCV000339036.1,