rs886043460

Orientation

plus

Stabilized

plus

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

Chromosome

5

Position

156594992

Gene

SGCD

is a	snp
is	mentioned by
dbSNP	rs886043460
dbSNP (classic)	rs886043460
ClinGen	rs886043460
ebi	rs886043460
HLI	rs886043460
Exac	rs886043460
Gnomad	rs886043460
Varsome	rs886043460
LitVar	rs886043460
Map	rs886043460
PheGenI	rs886043460
Biobank	rs886043460
1000 genomes	rs886043460
hgdp	rs886043460
ensembl	rs886043460
geneview	rs886043460
scholar	rs886043460
google	rs886043460
pharmgkb	rs886043460
gwascentral	rs886043460
openSNP	rs886043460
23andMe	rs886043460
SNPshot	rs886043460
SNPdbe	rs886043460
MSV3d	rs886043460
GWAS Ctlg	rs886043460

Max Magnitude

0

ClinVar
Risk	rs886043460(A;A)
Alt	rs886043460(A;A)
Reference	Rs886043460(T;T)
Significance	Pathogenic
Disease	Limb-girdle muscular dystrophy
Variation	info
Gene	SGCD
CLNDBN	Limb-girdle muscular dystrophy, type 2F
Reversed	0
HGVS	NC_000005.9:g.156022002T>A
CLNSRC
CLNACC	RCV000340742.1,