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rs796053362

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053362(G;T)
Make rs796053362(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127669899
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs796053362
ebirs796053362
HLIrs796053362
Exacrs796053362
Varsomers796053362
Maprs796053362
PheGenIrs796053362
hapmaprs796053362
1000 genomesrs796053362
hgdprs796053362
ensemblrs796053362
gopubmedrs796053362
geneviewrs796053362
scholarrs796053362
googlers796053362
pharmgkbrs796053362
gwascentralrs796053362
openSNPrs796053362
23andMers796053362
23andMe allrs796053362
SNP Nexus

SNPshotrs796053362
SNPdbers796053362
MSV3drs796053362
GWAS Ctlgrs796053362
Max Magnitude0
ClinVar
Risk rs796053362(T;T)
Alt rs796053362(T;T)
Reference rs796053362(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130432178G>T
CLNSRC
CLNACC RCV000189607.1,