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rs796053391

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053391(-;-)
Make rs796053391(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127680165
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs796053391
dbSNP (classic)rs796053391
ClinGenrs796053391
ebirs796053391
HLIrs796053391
Exacrs796053391
Gnomadrs796053391
Varsomers796053391
LitVarrs796053391
Maprs796053391
PheGenIrs796053391
Biobankrs796053391
1000 genomesrs796053391
hgdprs796053391
ensemblrs796053391
geneviewrs796053391
scholarrs796053391
googlers796053391
pharmgkbrs796053391
gwascentralrs796053391
openSNPrs796053391
23andMers796053391
SNPshotrs796053391
SNPdbers796053391
MSV3drs796053391
GWAS Ctlgrs796053391
Max Magnitude0
ClinVar
Risk rs796053391(-;-)
Alt rs796053391(-;-)
Reference Rs796053391(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130442444delT
CLNSRC
CLNACC RCV000189643.1,