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rs796053370

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053370(A;A)
Make rs796053370(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127676754
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs796053370
ebirs796053370
HLIrs796053370
Exacrs796053370
Varsomers796053370
Maprs796053370
PheGenIrs796053370
hapmaprs796053370
1000 genomesrs796053370
hgdprs796053370
ensemblrs796053370
gopubmedrs796053370
geneviewrs796053370
scholarrs796053370
googlers796053370
pharmgkbrs796053370
gwascentralrs796053370
openSNPrs796053370
23andMers796053370
23andMe allrs796053370
SNP Nexus

SNPshotrs796053370
SNPdbers796053370
MSV3drs796053370
GWAS Ctlgrs796053370
Max Magnitude0
ClinVar
Risk rs796053370(A;A)
Alt rs796053370(A;A)
Reference rs796053370(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130439033G>A
CLNSRC
CLNACC RCV000189618.1,