Have questions? Visit https://www.reddit.com/r/SNPedia

rs756623659

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs756623659(A;A)
Make rs756623659(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position1022225
GeneAGRN
is asnp
is mentioned by
dbSNPrs756623659
ebirs756623659
HLIrs756623659
Exacrs756623659
Varsomers756623659
Maprs756623659
PheGenIrs756623659
hapmaprs756623659
1000 genomesrs756623659
hgdprs756623659
ensemblrs756623659
gopubmedrs756623659
geneviewrs756623659
scholarrs756623659
googlers756623659
pharmgkbrs756623659
gwascentralrs756623659
openSNPrs756623659
23andMers756623659
23andMe allrs756623659
SNP Nexus

SNPshotrs756623659
SNPdbers756623659
MSV3drs756623659
GWAS Ctlgrs756623659
Max Magnitude0
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,