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rs587777782

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777782(A;A)
Make rs587777782(A;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position202599348
GeneSYT2
is asnp
is mentioned by
dbSNPrs587777782
ebirs587777782
HLIrs587777782
Exacrs587777782
Varsomers587777782
Maprs587777782
PheGenIrs587777782
hapmaprs587777782
1000 genomesrs587777782
hgdprs587777782
ensemblrs587777782
gopubmedrs587777782
geneviewrs587777782
scholarrs587777782
googlers587777782
pharmgkbrs587777782
gwascentralrs587777782
openSNPrs587777782
23andMers587777782
23andMe allrs587777782
SNP Nexus

SNPshotrs587777782
SNPdbers587777782
MSV3drs587777782
GWAS Ctlgrs587777782
Max Magnitude0
ClinVar
Risk rs587777782(A;A)
Alt rs587777782(A;A)
Reference rs587777782(G;G)
Significance Pathogenic
Disease Myasthenic syndrome
Variation info
Gene SYT2
CLNDBN Myasthenic syndrome, congenital, 7, presynaptic
Reversed 0
HGVS NC_000001.10:g.202568476G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144452.4,