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rs796053374

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053374(C;C)
Make rs796053374(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127682510
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs796053374
ebirs796053374
HLIrs796053374
Exacrs796053374
Varsomers796053374
Maprs796053374
PheGenIrs796053374
hapmaprs796053374
1000 genomesrs796053374
hgdprs796053374
ensemblrs796053374
gopubmedrs796053374
geneviewrs796053374
scholarrs796053374
googlers796053374
pharmgkbrs796053374
gwascentralrs796053374
openSNPrs796053374
23andMers796053374
23andMe allrs796053374
SNP Nexus

SNPshotrs796053374
SNPdbers796053374
MSV3drs796053374
GWAS Ctlgrs796053374
Max Magnitude0
ClinVar
Risk rs796053374(C;C)
Alt rs796053374(C;C)
Reference rs796053374(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130444789G>C
CLNSRC
CLNACC RCV000189624.2,