rs370819630

Orientation

plus

Stabilized

plus

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

Make rs370819630(A;G)

Make rs370819630(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

17

Position

50167731

Gene	LOC105371818, SGCA

is a	snp
is	mentioned by
dbSNP	rs370819630
dbSNP (classic)	rs370819630
ClinGen	rs370819630
ebi	rs370819630
HLI	rs370819630
Exac	rs370819630
Gnomad	rs370819630
Varsome	rs370819630
LitVar	rs370819630
Map	rs370819630
PheGenI	rs370819630
Biobank	rs370819630
1000 genomes	rs370819630
hgdp	rs370819630
ensembl	rs370819630
geneview	rs370819630
scholar	rs370819630
google	rs370819630
pharmgkb	rs370819630
gwascentral	rs370819630
openSNP	rs370819630
23andMe	rs370819630
SNPshot	rs370819630
SNPdbe	rs370819630
MSV3d	rs370819630
GWAS Ctlg	rs370819630

Max Magnitude

0

ClinVar
Risk	rs370819630(G;G)
Alt	rs370819630(G;G)
Reference	Rs370819630(A;A)
Significance	Probable-Pathogenic
Disease	Limb-girdle muscular dystrophy
Variation	info
Gene	SGCA
CLNDBN	Limb-girdle muscular dystrophy, type 2D
Reversed	0
HGVS	NC_000017.10:g.48245092A>G
CLNSRC
CLNACC	RCV000277867.1,