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rs879253787

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs879253787(A;T)
Make rs879253787(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position1022313
GeneAGRN
is asnp
is mentioned by
dbSNPrs879253787
ebirs879253787
HLIrs879253787
Exacrs879253787
Varsomers879253787
Maprs879253787
PheGenIrs879253787
hapmaprs879253787
1000 genomesrs879253787
hgdprs879253787
ensemblrs879253787
gopubmedrs879253787
geneviewrs879253787
scholarrs879253787
googlers879253787
pharmgkbrs879253787
gwascentralrs879253787
openSNPrs879253787
23andMers879253787
23andMe allrs879253787
SNP Nexus

SNPshotrs879253787
SNPdbers879253787
MSV3drs879253787
GWAS Ctlgrs879253787
Max Magnitude0
ClinVar
Risk rs879253787(T;T)
Alt rs879253787(T;T)
Reference rs879253787(A;A)
Significance Pathogenic
Disease Congenital myasthenic syndrome
Variation info
Gene AGRN
CLNDBN Congenital myasthenic syndrome
Reversed 0
HGVS NC_000001.10:g.957693A>T
CLNSRC
CLNACC RCV000235021.1,