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rs796053385

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796053385(-;A)
Make rs796053385(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127676690
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs796053385
ClinGenrs796053385
ebirs796053385
HLIrs796053385
Exacrs796053385
Varsomers796053385
Maprs796053385
PheGenIrs796053385
hapmaprs796053385
1000 genomesrs796053385
hgdprs796053385
ensemblrs796053385
gopubmedrs796053385
geneviewrs796053385
scholarrs796053385
googlers796053385
pharmgkbrs796053385
gwascentralrs796053385
openSNPrs796053385
23andMers796053385
23andMe allrs796053385
SNP Nexus

SNPshotrs796053385
SNPdbers796053385
MSV3drs796053385
GWAS Ctlgrs796053385
Max Magnitude0
ClinVar
Risk rs796053385(A;A)
Alt rs796053385(A;A)
Reference Rs796053385(;)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130438969dupA
CLNSRC
CLNACC RCV000189635.1,