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rs1009316

From SNPedia

Orientationplus
Stabilizedplus
Make rs1009316(C;C)
Make rs1009316(C;T)
Make rs1009316(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position48955313
GeneBAX
is asnp
is mentioned by
dbSNPrs1009316
dbSNP (classic)rs1009316
ClinGenrs1009316
ebirs1009316
HLIrs1009316
Exacrs1009316
Gnomadrs1009316
Varsomers1009316
LitVarrs1009316
Maprs1009316
PheGenIrs1009316
Biobankrs1009316
1000 genomesrs1009316
hgdprs1009316
ensemblrs1009316
geneviewrs1009316
scholarrs1009316
googlers1009316
pharmgkbrs1009316
gwascentralrs1009316
openSNPrs1009316
23andMers1009316
SNPshotrs1009316
SNPdbers1009316
MSV3drs1009316
GWAS Ctlgrs1009316
GMAF0.1644
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 24474449] Association between SNPs in P53 binding regions and risk of esophageal squamous cell carcinoma