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rs796053350

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053350(A;A)
Make rs796053350(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127651653
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs796053350
ebirs796053350
HLIrs796053350
Exacrs796053350
Varsomers796053350
Maprs796053350
PheGenIrs796053350
hapmaprs796053350
1000 genomesrs796053350
hgdprs796053350
ensemblrs796053350
gopubmedrs796053350
geneviewrs796053350
scholarrs796053350
googlers796053350
pharmgkbrs796053350
gwascentralrs796053350
openSNPrs796053350
23andMers796053350
23andMe allrs796053350
SNP Nexus

SNPshotrs796053350
SNPdbers796053350
MSV3drs796053350
GWAS Ctlgrs796053350
Max Magnitude0
ClinVar
Risk rs796053350(A;A)
Alt rs796053350(A;A)
Reference rs796053350(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130413932G>A
CLNSRC
CLNACC RCV000189593.1,