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rs794727970

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794727970(A;A)
Make rs794727970(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome9
Position127666206
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs794727970
dbSNP (classic)rs794727970
ClinGenrs794727970
ebirs794727970
HLIrs794727970
Exacrs794727970
Gnomadrs794727970
Varsomers794727970
LitVarrs794727970
Maprs794727970
PheGenIrs794727970
Biobankrs794727970
1000 genomesrs794727970
hgdprs794727970
ensemblrs794727970
geneviewrs794727970
scholarrs794727970
googlers794727970
pharmgkbrs794727970
gwascentralrs794727970
openSNPrs794727970
23andMers794727970
SNPshotrs794727970
SNPdbers794727970
MSV3drs794727970
GWAS Ctlgrs794727970
Max Magnitude0
ClinVar
Risk rs794727970(A;A)
Alt rs794727970(A;A)
Reference Rs794727970(G;G)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene STXBP1
CLNDBN not provided not specified
Reversed 0
HGVS NC_000009.11:g.130428485G>A
CLNSRC
CLNACC RCV000180590.4, RCV000259191.1,