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rs796053373

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053373(A;A)
Make rs796053373(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127682509
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs796053373
ebirs796053373
HLIrs796053373
Exacrs796053373
Varsomers796053373
Maprs796053373
PheGenIrs796053373
hapmaprs796053373
1000 genomesrs796053373
hgdprs796053373
ensemblrs796053373
gopubmedrs796053373
geneviewrs796053373
scholarrs796053373
googlers796053373
pharmgkbrs796053373
gwascentralrs796053373
openSNPrs796053373
23andMers796053373
23andMe allrs796053373
SNP Nexus

SNPshotrs796053373
SNPdbers796053373
MSV3drs796053373
GWAS Ctlgrs796053373
Max Magnitude0
ClinVar
Risk rs796053373(A,T;A,T)
Alt rs796053373(A,T;A,T)
Reference rs796053373(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130444788C>A; NC_000009.11:g.130444788C>T
CLNSRC
CLNACC RCV000189622.2, RCV000189623.2,