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rs796053356

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053356(A;A)
Make rs796053356(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127663344
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs796053356
ebirs796053356
HLIrs796053356
Exacrs796053356
Varsomers796053356
Maprs796053356
PheGenIrs796053356
hapmaprs796053356
1000 genomesrs796053356
hgdprs796053356
ensemblrs796053356
gopubmedrs796053356
geneviewrs796053356
scholarrs796053356
googlers796053356
pharmgkbrs796053356
gwascentralrs796053356
openSNPrs796053356
23andMers796053356
23andMe allrs796053356
SNP Nexus

SNPshotrs796053356
SNPdbers796053356
MSV3drs796053356
GWAS Ctlgrs796053356
Max Magnitude0
ClinVar
Risk rs796053356(A;A)
Alt rs796053356(A;A)
Reference rs796053356(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130425623G>A
CLNSRC
CLNACC RCV000189600.2,