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rs1057518154

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs1057518154(-;-)
Make rs1057518154(-;CT)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position127673246
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs1057518154
dbSNP (old)rs1057518154
ClinGenrs1057518154
ebirs1057518154
HLIrs1057518154
Exacrs1057518154
Gnomadrs1057518154
Varsomers1057518154
Maprs1057518154
PheGenIrs1057518154
Biobankrs1057518154
1000 genomesrs1057518154
hgdprs1057518154
ensemblrs1057518154
gopubmedrs1057518154
geneviewrs1057518154
scholarrs1057518154
googlers1057518154
pharmgkbrs1057518154
gwascentralrs1057518154
openSNPrs1057518154
23andMers1057518154
23andMe allrs1057518154
SNPshotrs1057518154
SNPdbers1057518154
MSV3drs1057518154
GWAS Ctlgrs1057518154
Max Magnitude0
ClinVar
Risk rs1057518154(-;-)
Alt rs1057518154(-;-)
Reference Rs1057518154(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130435525_130435526delCT
CLNSRC
CLNACC RCV000413787.1,