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rs796053360

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053360(A;A)
Make rs796053360(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127668079
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs796053360
ClinGenrs796053360
ebirs796053360
HLIrs796053360
Exacrs796053360
Varsomers796053360
Maprs796053360
PheGenIrs796053360
hapmaprs796053360
1000 genomesrs796053360
hgdprs796053360
ensemblrs796053360
gopubmedrs796053360
geneviewrs796053360
scholarrs796053360
googlers796053360
pharmgkbrs796053360
gwascentralrs796053360
openSNPrs796053360
23andMers796053360
23andMe allrs796053360
SNP Nexus

SNPshotrs796053360
SNPdbers796053360
MSV3drs796053360
GWAS Ctlgrs796053360
Max Magnitude0
ClinVar
Risk rs796053360(A;A)
Alt rs796053360(A;A)
Reference Rs796053360(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130430358G>A
CLNSRC
CLNACC RCV000189605.1,