rs121909298

Orientation

plus

Stabilized

plus

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

Make rs121909298(G;G)

Make rs121909298(G;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

156595000

Gene

SGCD

is a	snp
is	mentioned by
dbSNP	rs121909298
dbSNP (classic)	rs121909298
ClinGen	rs121909298
ebi	rs121909298
HLI	rs121909298
Exac	rs121909298
Gnomad	rs121909298
Varsome	rs121909298
LitVar	rs121909298
Map	rs121909298
PheGenI	rs121909298
Biobank	rs121909298
1000 genomes	rs121909298
hgdp	rs121909298
ensembl	rs121909298
geneview	rs121909298
scholar	rs121909298
google	rs121909298
pharmgkb	rs121909298
gwascentral	rs121909298
openSNP	rs121909298
23andMe	rs121909298
SNPshot	rs121909298
SNPdbe	rs121909298
MSV3d	rs121909298
GWAS Ctlg	rs121909298

Max Magnitude

0

OMIM	601411
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121909298(G;G)
Alt	rs121909298(G;G)
Reference	Rs121909298(T;T)
Significance	Other
Disease	Dilated cardiomyopathy 1L Muscular dystrophy not specified
Variation	info
Gene	SGCD
CLNDBN	Dilated cardiomyopathy 1L Muscular dystrophy, limb-girdle, type 2F, digenic not specified
Reversed	0
HGVS	NC_000005.9:g.156022010T>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008654.5, RCV000008655.3, RCV000041407.4,