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rs796053352

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053352(A;G)
Make rs796053352(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127658429
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs796053352
ebirs796053352
HLIrs796053352
Exacrs796053352
Varsomers796053352
Maprs796053352
PheGenIrs796053352
hapmaprs796053352
1000 genomesrs796053352
hgdprs796053352
ensemblrs796053352
gopubmedrs796053352
geneviewrs796053352
scholarrs796053352
googlers796053352
pharmgkbrs796053352
gwascentralrs796053352
openSNPrs796053352
23andMers796053352
23andMe allrs796053352
SNP Nexus

SNPshotrs796053352
SNPdbers796053352
MSV3drs796053352
GWAS Ctlgrs796053352
Max Magnitude0
ClinVar
Risk rs796053352(G;G)
Alt rs796053352(G;G)
Reference rs796053352(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130420708A>G
CLNSRC
CLNACC RCV000189596.1,