Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057524834

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524834(C;C)
Make rs1057524834(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position127666269
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs1057524834
dbSNP (old)rs1057524834
ClinGenrs1057524834
ebirs1057524834
HLIrs1057524834
Exacrs1057524834
Gnomadrs1057524834
Varsomers1057524834
LitVarrs1057524834
Maprs1057524834
PheGenIrs1057524834
Biobankrs1057524834
1000 genomesrs1057524834
hgdprs1057524834
ensemblrs1057524834
gopubmedrs1057524834
geneviewrs1057524834
scholarrs1057524834
googlers1057524834
pharmgkbrs1057524834
gwascentralrs1057524834
openSNPrs1057524834
23andMers1057524834
23andMe allrs1057524834
SNPshotrs1057524834
SNPdbers1057524834
MSV3drs1057524834
GWAS Ctlgrs1057524834
Max Magnitude0
ClinVar
Risk rs1057524834(C;C)
Alt rs1057524834(C;C)
Reference Rs1057524834(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130428548T>C
CLNSRC
CLNACC RCV000444312.1,