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rs200533370

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs200533370(C;C)
Make rs200533370(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position47574285
GeneSYN1
is asnp
is mentioned by
dbSNPrs200533370
ebirs200533370
HLIrs200533370
Exacrs200533370
Varsomers200533370
Maprs200533370
PheGenIrs200533370
hapmaprs200533370
1000 genomesrs200533370
hgdprs200533370
ensemblrs200533370
gopubmedrs200533370
geneviewrs200533370
scholarrs200533370
googlers200533370
pharmgkbrs200533370
gwascentralrs200533370
openSNPrs200533370
23andMers200533370
23andMe allrs200533370
SNP Nexus

SNPshotrs200533370
SNPdbers200533370
MSV3drs200533370
GWAS Ctlgrs200533370
Max Magnitude0
ClinVar
Risk rs200533370(C;C)
Alt rs200533370(C;C)
Reference rs200533370(T;T)
Significance Other
Disease Epilepsy not specified
Variation info
Gene SYN1
CLNDBN Epilepsy, X-linked, with variable learning disabilities and behavior disorders not specified
Reversed 0
HGVS NC_000023.10:g.47433684T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000034817.4, RCV000174415.2,