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rs1853665

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs1853665(A;A)
Make rs1853665(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position149977706
GeneLOC100506038
is asnp
is mentioned by
dbSNPrs1853665
dbSNP (classic)rs1853665
ClinGenrs1853665
ebirs1853665
HLIrs1853665
Exacrs1853665
Gnomadrs1853665
Varsomers1853665
LitVarrs1853665
Maprs1853665
PheGenIrs1853665
Biobankrs1853665
1000 genomesrs1853665
hgdprs1853665
ensemblrs1853665
geneviewrs1853665
scholarrs1853665
googlers1853665
pharmgkbrs1853665
gwascentralrs1853665
openSNPrs1853665
23andMers1853665
SNPshotrs1853665
SNPdbers1853665
MSV3drs1853665
GWAS Ctlgrs1853665
GMAF0.2957
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 20923822OA-icon.png]
Trait
Title Radiation pharmacogenomics: A genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines
Risk Allele
P-val 0.000007
Odds Ratio None None