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rs805510

From SNPedia

Orientationminus
Make rs805510(A;A)
Make rs805510(A;G)
Make rs805510(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position27986913
is asnp
is mentioned by
dbSNPrs805510
ebirs805510
HLIrs805510
Exacrs805510
Varsomers805510
Maprs805510
PheGenIrs805510
hapmaprs805510
1000 genomesrs805510
hgdprs805510
ensemblrs805510
gopubmedrs805510
geneviewrs805510
scholarrs805510
googlers805510
pharmgkbrs805510
gwascentralrs805510
openSNPrs805510
23andMers805510
23andMe allrs805510
SNP Nexus

SNPshotrs805510
SNPdbers805510
MSV3drs805510
GWAS Ctlgrs805510
Max Magnitude
? (A;A) (A;G) (G;G) 28

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