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rs796053387

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053387(C;G)
Make rs796053387(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127653794
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs796053387
ebirs796053387
HLIrs796053387
Exacrs796053387
Varsomers796053387
Maprs796053387
PheGenIrs796053387
hapmaprs796053387
1000 genomesrs796053387
hgdprs796053387
ensemblrs796053387
gopubmedrs796053387
geneviewrs796053387
scholarrs796053387
googlers796053387
pharmgkbrs796053387
gwascentralrs796053387
openSNPrs796053387
23andMers796053387
23andMe allrs796053387
SNP Nexus

SNPshotrs796053387
SNPdbers796053387
MSV3drs796053387
GWAS Ctlgrs796053387
Max Magnitude0
ClinVar
Risk rs796053387(G;G)
Alt rs796053387(G;G)
Reference rs796053387(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130416073C>G
CLNSRC
CLNACC RCV000189637.1,