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rs1057518167

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518167(-;A)
Make rs1057518167(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position127653775
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs1057518167
dbSNP (old)rs1057518167
ClinGenrs1057518167
ebirs1057518167
HLIrs1057518167
Exacrs1057518167
Gnomadrs1057518167
Varsomers1057518167
LitVarrs1057518167
Maprs1057518167
PheGenIrs1057518167
Biobankrs1057518167
1000 genomesrs1057518167
hgdprs1057518167
ensemblrs1057518167
gopubmedrs1057518167
geneviewrs1057518167
scholarrs1057518167
googlers1057518167
pharmgkbrs1057518167
gwascentralrs1057518167
openSNPrs1057518167
23andMers1057518167
23andMe allrs1057518167
SNPshotrs1057518167
SNPdbers1057518167
MSV3drs1057518167
GWAS Ctlgrs1057518167
Max Magnitude0
ClinVar
Risk rs1057518167(A;A)
Alt rs1057518167(A;A)
Reference Rs1057518167(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130416054dupA
CLNSRC
CLNACC RCV000413558.1,