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rs1057524795

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524795(C;T)
Make rs1057524795(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position127666245
GeneSTXBP1
is asnp
is mentioned by
dbSNPrs1057524795
dbSNP (classic)rs1057524795
ClinGenrs1057524795
ebirs1057524795
HLIrs1057524795
Exacrs1057524795
Gnomadrs1057524795
Varsomers1057524795
LitVarrs1057524795
Maprs1057524795
PheGenIrs1057524795
Biobankrs1057524795
1000 genomesrs1057524795
hgdprs1057524795
ensemblrs1057524795
geneviewrs1057524795
scholarrs1057524795
googlers1057524795
pharmgkbrs1057524795
gwascentralrs1057524795
openSNPrs1057524795
23andMers1057524795
23andMe allrs1057524795
SNPshotrs1057524795
SNPdbers1057524795
MSV3drs1057524795
GWAS Ctlgrs1057524795
Max Magnitude0
ClinVar
Risk rs1057524795(T;T)
Alt rs1057524795(T;T)
Reference Rs1057524795(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene STXBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130428524C>T
CLNSRC
CLNACC RCV000436434.1,