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

rs1057520631

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520631(A;A)
Make rs1057520631(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position127666301
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs1057520631
dbSNP (old)rs1057520631
ClinGenrs1057520631
ebirs1057520631
HLIrs1057520631
Exacrs1057520631
Gnomadrs1057520631
Varsomers1057520631
LitVarrs1057520631
Maprs1057520631
PheGenIrs1057520631
Biobankrs1057520631
1000 genomesrs1057520631
hgdprs1057520631
ensemblrs1057520631
gopubmedrs1057520631
geneviewrs1057520631
scholarrs1057520631
googlers1057520631
pharmgkbrs1057520631
gwascentralrs1057520631
openSNPrs1057520631
23andMers1057520631
23andMe allrs1057520631
SNPshotrs1057520631
SNPdbers1057520631
MSV3drs1057520631
GWAS Ctlgrs1057520631
Max Magnitude0
ClinVar
Risk rs1057520631(A;A)
Alt rs1057520631(A;A)
Reference Rs1057520631(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130428580G>A
CLNSRC
CLNACC RCV000444271.1,