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rs796053355

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053355(C;T)
Make rs796053355(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127663343
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs796053355
ebirs796053355
HLIrs796053355
Exacrs796053355
Varsomers796053355
Maprs796053355
PheGenIrs796053355
hapmaprs796053355
1000 genomesrs796053355
hgdprs796053355
ensemblrs796053355
gopubmedrs796053355
geneviewrs796053355
scholarrs796053355
googlers796053355
pharmgkbrs796053355
gwascentralrs796053355
openSNPrs796053355
23andMers796053355
23andMe allrs796053355
SNP Nexus

SNPshotrs796053355
SNPdbers796053355
MSV3drs796053355
GWAS Ctlgrs796053355
Max Magnitude0
ClinVar
Risk rs796053355(T;T)
Alt rs796053355(T;T)
Reference rs796053355(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130425622C>T
CLNSRC
CLNACC RCV000189599.2,