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rs763818876

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs763818876(A;A)
Make rs763818876(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position1051775
GeneAGRN
is asnp
is mentioned by
dbSNPrs763818876
ebirs763818876
HLIrs763818876
Exacrs763818876
Varsomers763818876
Maprs763818876
PheGenIrs763818876
hapmaprs763818876
1000 genomesrs763818876
hgdprs763818876
ensemblrs763818876
gopubmedrs763818876
geneviewrs763818876
scholarrs763818876
googlers763818876
pharmgkbrs763818876
gwascentralrs763818876
openSNPrs763818876
23andMers763818876
23andMe allrs763818876
SNP Nexus

SNPshotrs763818876
SNPdbers763818876
MSV3drs763818876
GWAS Ctlgrs763818876
Max Magnitude0
ClinVar
Risk rs763818876(A;A)
Alt rs763818876(A;A)
Reference rs763818876(G;G)
Significance Pathogenic
Disease Congenital myasthenic syndrome
Variation info
Gene AGRN
CLNDBN Congenital myasthenic syndrome
Reversed 0
HGVS NC_000001.10:g.987155G>A
CLNSRC
CLNACC RCV000235024.1,