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

rs1381392

From SNPedia

Orientationminus
Stabilizedminus
Make rs1381392(C;C)
Make rs1381392(C;T)
Make rs1381392(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position28707823
GeneLINC00693
is asnp
is mentioned by
dbSNPrs1381392
dbSNP (classic)rs1381392
ClinGenrs1381392
ebirs1381392
HLIrs1381392
Exacrs1381392
Gnomadrs1381392
Varsomers1381392
LitVarrs1381392
Maprs1381392
PheGenIrs1381392
Biobankrs1381392
1000 genomesrs1381392
hgdprs1381392
ensemblrs1381392
geneviewrs1381392
scholarrs1381392
googlers1381392
pharmgkbrs1381392
gwascentralrs1381392
openSNPrs1381392
23andMers1381392
SNPshotrs1381392
SNPdbers1381392
MSV3drs1381392
GWAS Ctlgrs1381392
GMAF0.118
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 24084763OA-icon.png] Germline Variants and Advanced Colorectal Adenomas: Adenoma Prevention with Celecoxib Trial Genomewide Association Study


[PMID 19299336OA-icon.png] Genome-wide association study to identify novel loci associated with therapy-related myeloid leukemia susceptibility.