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rs1057517880

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517880(C;T)
Make rs1057517880(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position127668162
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs1057517880
dbSNP (classic)rs1057517880
ClinGenrs1057517880
ebirs1057517880
HLIrs1057517880
Exacrs1057517880
Gnomadrs1057517880
Varsomers1057517880
LitVarrs1057517880
Maprs1057517880
PheGenIrs1057517880
Biobankrs1057517880
1000 genomesrs1057517880
hgdprs1057517880
ensemblrs1057517880
geneviewrs1057517880
scholarrs1057517880
googlers1057517880
pharmgkbrs1057517880
gwascentralrs1057517880
openSNPrs1057517880
23andMers1057517880
23andMe allrs1057517880
SNPshotrs1057517880
SNPdbers1057517880
MSV3drs1057517880
GWAS Ctlgrs1057517880
Max Magnitude0
ClinVar
Risk rs1057517880(T;T)
Alt rs1057517880(T;T)
Reference Rs1057517880(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130430441C>T
CLNSRC
CLNACC RCV000414192.1,