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rs796053379

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053379(A;T)
Make rs796053379(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127612443
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs796053379
ebirs796053379
HLIrs796053379
Exacrs796053379
Varsomers796053379
Maprs796053379
PheGenIrs796053379
hapmaprs796053379
1000 genomesrs796053379
hgdprs796053379
ensemblrs796053379
gopubmedrs796053379
geneviewrs796053379
scholarrs796053379
googlers796053379
pharmgkbrs796053379
gwascentralrs796053379
openSNPrs796053379
23andMers796053379
23andMe allrs796053379
SNP Nexus

SNPshotrs796053379
SNPdbers796053379
MSV3drs796053379
GWAS Ctlgrs796053379
Max Magnitude0
ClinVar
Risk rs796053379(T;T)
Alt rs796053379(T;T)
Reference rs796053379(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130374722A>T
CLNSRC
CLNACC RCV000189629.2,