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rs796053390

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs796053390(-;-)
Make rs796053390(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127661164
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs796053390
ClinGenrs796053390
ebirs796053390
HLIrs796053390
Exacrs796053390
Varsomers796053390
Maprs796053390
PheGenIrs796053390
hapmaprs796053390
1000 genomesrs796053390
hgdprs796053390
ensemblrs796053390
gopubmedrs796053390
geneviewrs796053390
scholarrs796053390
googlers796053390
pharmgkbrs796053390
gwascentralrs796053390
openSNPrs796053390
23andMers796053390
23andMe allrs796053390
SNP Nexus

SNPshotrs796053390
SNPdbers796053390
MSV3drs796053390
GWAS Ctlgrs796053390
Max Magnitude0
ClinVar
Risk rs796053390(-;-)
Alt rs796053390(-;-)
Reference Rs796053390(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130423443_130423444delCT
CLNSRC
CLNACC RCV000189641.1,