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rs1057523381

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057523381(A;G)
Make rs1057523381(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position127682500
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs1057523381
dbSNP (old)rs1057523381
ClinGenrs1057523381
ebirs1057523381
HLIrs1057523381
Exacrs1057523381
Gnomadrs1057523381
Varsomers1057523381
Maprs1057523381
PheGenIrs1057523381
Biobankrs1057523381
1000 genomesrs1057523381
hgdprs1057523381
ensemblrs1057523381
gopubmedrs1057523381
geneviewrs1057523381
scholarrs1057523381
googlers1057523381
pharmgkbrs1057523381
gwascentralrs1057523381
openSNPrs1057523381
23andMers1057523381
23andMe allrs1057523381
SNPshotrs1057523381
SNPdbers1057523381
MSV3drs1057523381
GWAS Ctlgrs1057523381
Max Magnitude0
ClinVar
Risk rs1057523381(G;G)
Alt rs1057523381(G;G)
Reference Rs1057523381(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130444779A>G
CLNSRC
CLNACC RCV000430934.1,