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rs6949149

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs6949149(G;T)
Make rs6949149(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position22709538
is asnp
is mentioned by
dbSNPrs6949149
dbSNP (classic)rs6949149
ClinGenrs6949149
ebirs6949149
HLIrs6949149
Exacrs6949149
Gnomadrs6949149
Varsomers6949149
LitVarrs6949149
Maprs6949149
PheGenIrs6949149
Biobankrs6949149
1000 genomesrs6949149
hgdprs6949149
ensemblrs6949149
geneviewrs6949149
scholarrs6949149
googlers6949149
pharmgkbrs6949149
gwascentralrs6949149
openSNPrs6949149
23andMers6949149
SNPshotrs6949149
SNPdbers6949149
MSV3drs6949149
GWAS Ctlgrs6949149
GMAF0.2631
Max Magnitude0
? (G;G) (G;T) (T;T) 28


[PMID 19965896OA-icon.png] PTGS2 and IL6 Genetic Variation and Risk of Breast and Prostate Cancer: results from the Breast and Prostate Cancer Cohort Consortium (BPC3)