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rs796053375

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053375(G;T)
Make rs796053375(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127682521
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs796053375
ebirs796053375
HLIrs796053375
Exacrs796053375
Varsomers796053375
Maprs796053375
PheGenIrs796053375
hapmaprs796053375
1000 genomesrs796053375
hgdprs796053375
ensemblrs796053375
gopubmedrs796053375
geneviewrs796053375
scholarrs796053375
googlers796053375
pharmgkbrs796053375
gwascentralrs796053375
openSNPrs796053375
23andMers796053375
23andMe allrs796053375
SNP Nexus

SNPshotrs796053375
SNPdbers796053375
MSV3drs796053375
GWAS Ctlgrs796053375
Max Magnitude0
ClinVar
Risk rs796053375(T;T)
Alt rs796053375(T;T)
Reference rs796053375(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130444800G>T
CLNSRC
CLNACC RCV000189625.1,