rs4770403

Orientation

plus

Stabilized

plus

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

Make rs4770403(A;A)

Make rs4770403(A;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

23180988

Gene

SGCG

is a	snp
is	mentioned by
dbSNP	rs4770403
dbSNP (classic)	rs4770403
ClinGen	rs4770403
ebi	rs4770403
HLI	rs4770403
Exac	rs4770403
Gnomad	rs4770403
Varsome	rs4770403
LitVar	rs4770403
Map	rs4770403
PheGenI	rs4770403
Biobank	rs4770403
1000 genomes	rs4770403
hgdp	rs4770403
ensembl	rs4770403
geneview	rs4770403
scholar	rs4770403
google	rs4770403
pharmgkb	rs4770403
gwascentral	rs4770403
openSNP	rs4770403
23andMe	rs4770403
SNPshot	rs4770403
SNPdbe	rs4770403
MSV3d	rs4770403
GWAS Ctlg	rs4770403

GMAF

0.1497

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 22004471]
Trait
Title	Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster.
Risk Allele
P-val	0.000006
Odds Ratio	1.3300 None

ClinVar
Risk	rs4770403(A;A)
Alt	rs4770403(A;A)
Reference	Rs4770403(G;G)
Significance	Probable-non-pathogenic
Disease	Limb-Girdle Muscular Dystrophy Severe autosomal recessive muscular dystrophy of childhood - North African type
Variation	info
Gene	SGCG
CLNDBN	Limb-Girdle Muscular Dystrophy, Recessive Severe autosomal recessive muscular dystrophy of childhood - North African type
Reversed	0
HGVS	NC_000013.10:g.23755127G>A
CLNSRC
CLNACC	RCV000295084.1, RCV000336138.1,