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rs796053382

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796053382(-;G)
Make rs796053382(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127663354
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs796053382
dbSNP (old)rs796053382
ClinGenrs796053382
ebirs796053382
HLIrs796053382
Exacrs796053382
Gnomadrs796053382
Varsomers796053382
Maprs796053382
PheGenIrs796053382
Biobankrs796053382
1000 genomesrs796053382
hgdprs796053382
ensemblrs796053382
gopubmedrs796053382
geneviewrs796053382
scholarrs796053382
googlers796053382
pharmgkbrs796053382
gwascentralrs796053382
openSNPrs796053382
23andMers796053382
23andMe allrs796053382
SNP Nexus

SNPshotrs796053382
SNPdbers796053382
MSV3drs796053382
GWAS Ctlgrs796053382
Max Magnitude0
ClinVar
Risk rs796053382(G;G)
Alt rs796053382(G;G)
Reference Rs796053382(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130425633dupG
CLNSRC
CLNACC RCV000189632.1,