rs764160563

Orientation

plus

Stabilized

plus

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

Make rs764160563(A;A)

Make rs764160563(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

1050473

Gene

AGRN

is a	snp
is	mentioned by
dbSNP	rs764160563
dbSNP (classic)	rs764160563
ClinGen	rs764160563
ebi	rs764160563
HLI	rs764160563
Exac	rs764160563
Gnomad	rs764160563
Varsome	rs764160563
LitVar	rs764160563
Map	rs764160563
PheGenI	rs764160563
Biobank	rs764160563
1000 genomes	rs764160563
hgdp	rs764160563
ensembl	rs764160563
geneview	rs764160563
scholar	rs764160563
google	rs764160563
pharmgkb	rs764160563
gwascentral	rs764160563
openSNP	rs764160563
23andMe	rs764160563
SNPshot	rs764160563
SNPdbe	rs764160563
MSV3d	rs764160563
GWAS Ctlg	rs764160563

Max Magnitude

0

ClinVar
Risk	rs764160563(A;A)
Alt	rs764160563(A;A)
Reference	Rs764160563(G;G)
Significance	Pathogenic
Disease	Congenital myasthenic syndrome
Variation	info
Gene	AGRN
CLNDBN	Congenital myasthenic syndrome
Reversed	0
HGVS	NC_000001.10:g.985853G>A
CLNSRC
CLNACC	RCV000235025.1,