rs756623659

Orientation

plus

Stabilized

plus

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

Make rs756623659(A;A)

Make rs756623659(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

1022225

Gene

AGRN

is a	snp
is	mentioned by
dbSNP	rs756623659
dbSNP (classic)	rs756623659
ClinGen	rs756623659
ebi	rs756623659
HLI	rs756623659
Exac	rs756623659
Gnomad	rs756623659
Varsome	rs756623659
LitVar	rs756623659
Map	rs756623659
PheGenI	rs756623659
Biobank	rs756623659
1000 genomes	rs756623659
hgdp	rs756623659
ensembl	rs756623659
geneview	rs756623659
scholar	rs756623659
google	rs756623659
pharmgkb	rs756623659
gwascentral	rs756623659
openSNP	rs756623659
23andMe	rs756623659
SNPshot	rs756623659
SNPdbe	rs756623659
MSV3d	rs756623659
GWAS Ctlg	rs756623659

Max Magnitude

0

ClinVar
Risk	rs756623659(A;A)
Alt	rs756623659(A;A)
Reference	Rs756623659(G;G)
Significance	Pathogenic
Disease	Congenital myasthenic syndrome
Variation	info
Gene	AGRN
CLNDBN	Congenital myasthenic syndrome
Reversed	0
HGVS	NC_000001.10:g.957605G>A
CLNSRC
CLNACC	RCV000235037.1,