rs372210292

Orientation

plus

Stabilized

plus

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

Make rs372210292(A;A)

Make rs372210292(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

17

Position

50168397

Gene	LOC105371818, SGCA

is a	snp
is	mentioned by
dbSNP	rs372210292
dbSNP (classic)	rs372210292
ClinGen	rs372210292
ebi	rs372210292
HLI	rs372210292
Exac	rs372210292
Gnomad	rs372210292
Varsome	rs372210292
LitVar	rs372210292
Map	rs372210292
PheGenI	rs372210292
Biobank	rs372210292
1000 genomes	rs372210292
hgdp	rs372210292
ensembl	rs372210292
geneview	rs372210292
scholar	rs372210292
google	rs372210292
pharmgkb	rs372210292
gwascentral	rs372210292
openSNP	rs372210292
23andMe	rs372210292
SNPshot	rs372210292
SNPdbe	rs372210292
MSV3d	rs372210292
GWAS Ctlg	rs372210292

Max Magnitude

0

ClinVar
Risk	rs372210292(A;A)
Alt	rs372210292(A;A)
Reference	Rs372210292(G;G)
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.48245758G>A
CLNSRC
CLNACC	RCV000341255.1,