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rs796053393

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053393(-;-)
Make rs796053393(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127690798
GeneMIR3911, STXBP1
is asnp
is mentioned by
dbSNPrs796053393
ClinGenrs796053393
ebirs796053393
HLIrs796053393
Exacrs796053393
Varsomers796053393
Maprs796053393
PheGenIrs796053393
hapmaprs796053393
1000 genomesrs796053393
hgdprs796053393
ensemblrs796053393
gopubmedrs796053393
geneviewrs796053393
scholarrs796053393
googlers796053393
pharmgkbrs796053393
gwascentralrs796053393
openSNPrs796053393
23andMers796053393
23andMe allrs796053393
SNP Nexus

SNPshotrs796053393
SNPdbers796053393
MSV3drs796053393
GWAS Ctlgrs796053393
Max Magnitude0
ClinVar
Risk rs796053393(-;-)
Alt rs796053393(-;-)
Reference Rs796053393(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1 MIR3911
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130453077delC
CLNSRC
CLNACC RCV000189645.1,