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rs113824616

From SNPedia

Orientationplus
Stabilizedplus
Make rs113824616(C;C)
Make rs113824616(C;T)
Make rs113824616(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position28031972
is asnp
is mentioned by
dbSNPrs113824616
dbSNP (old)rs113824616
ClinGenrs113824616
ebirs113824616
HLIrs113824616
Exacrs113824616
Varsomers113824616
Maprs113824616
PheGenIrs113824616
Biobankrs113824616
1000 genomesrs113824616
hgdprs113824616
ensemblrs113824616
gopubmedrs113824616
geneviewrs113824616
scholarrs113824616
googlers113824616
pharmgkbrs113824616
gwascentralrs113824616
openSNPrs113824616
23andMers113824616
23andMe allrs113824616
SNP Nexus

SNPshotrs113824616
SNPdbers113824616
MSV3drs113824616
GWAS Ctlgrs113824616
Max Magnitude

[PMID 27459855OA-icon.png] Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus.