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rs1057522982

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057522982(A;G)
Make rs1057522982(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position127678429
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs1057522982
dbSNP (old)rs1057522982
ClinGenrs1057522982
ebirs1057522982
HLIrs1057522982
Exacrs1057522982
Gnomadrs1057522982
Varsomers1057522982
LitVarrs1057522982
Maprs1057522982
PheGenIrs1057522982
Biobankrs1057522982
1000 genomesrs1057522982
hgdprs1057522982
ensemblrs1057522982
gopubmedrs1057522982
geneviewrs1057522982
scholarrs1057522982
googlers1057522982
pharmgkbrs1057522982
gwascentralrs1057522982
openSNPrs1057522982
23andMers1057522982
23andMe allrs1057522982
SNPshotrs1057522982
SNPdbers1057522982
MSV3drs1057522982
GWAS Ctlgrs1057522982
Max Magnitude0
ClinVar
Risk rs1057522982(G;G)
Alt rs1057522982(G;G)
Reference Rs1057522982(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130440708A>G
CLNSRC
CLNACC RCV000438565.1,