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rs796053377

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053377(A;A)
Make rs796053377(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127682561
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs796053377
ebirs796053377
HLIrs796053377
Exacrs796053377
Varsomers796053377
Maprs796053377
PheGenIrs796053377
hapmaprs796053377
1000 genomesrs796053377
hgdprs796053377
ensemblrs796053377
gopubmedrs796053377
geneviewrs796053377
scholarrs796053377
googlers796053377
pharmgkbrs796053377
gwascentralrs796053377
openSNPrs796053377
23andMers796053377
23andMe allrs796053377
SNP Nexus

SNPshotrs796053377
SNPdbers796053377
MSV3drs796053377
GWAS Ctlgrs796053377
Max Magnitude0
ClinVar
Risk rs796053377(A;A)
Alt rs796053377(A;A)
Reference rs796053377(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130444840G>A
CLNSRC
CLNACC RCV000189627.1,