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rs796053365

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053365(A;A)
Make rs796053365(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127673212
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs796053365
ebirs796053365
HLIrs796053365
Exacrs796053365
Varsomers796053365
Maprs796053365
PheGenIrs796053365
hapmaprs796053365
1000 genomesrs796053365
hgdprs796053365
ensemblrs796053365
gopubmedrs796053365
geneviewrs796053365
scholarrs796053365
googlers796053365
pharmgkbrs796053365
gwascentralrs796053365
openSNPrs796053365
23andMers796053365
23andMe allrs796053365
SNP Nexus

SNPshotrs796053365
SNPdbers796053365
MSV3drs796053365
GWAS Ctlgrs796053365
Max Magnitude0
ClinVar
Risk rs796053365(A;A)
Alt rs796053365(A;A)
Reference rs796053365(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130435491G>A
CLNSRC
CLNACC RCV000189610.1,