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rs796053357

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053357(G;T)
Make rs796053357(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127663354
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs796053357
ebirs796053357
HLIrs796053357
Exacrs796053357
Varsomers796053357
Maprs796053357
PheGenIrs796053357
hapmaprs796053357
1000 genomesrs796053357
hgdprs796053357
ensemblrs796053357
gopubmedrs796053357
geneviewrs796053357
scholarrs796053357
googlers796053357
pharmgkbrs796053357
gwascentralrs796053357
openSNPrs796053357
23andMers796053357
23andMe allrs796053357
SNP Nexus

SNPshotrs796053357
SNPdbers796053357
MSV3drs796053357
GWAS Ctlgrs796053357
Max Magnitude0
ClinVar
Risk rs796053357(T;T)
Alt rs796053357(T;T)
Reference rs796053357(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130425633G>T
CLNSRC
CLNACC RCV000189601.1,