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rs6864776

From SNPedia

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Make rs6864776(A;G)
Make rs6864776(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position44513202
GeneLOC102723839
is asnp
is mentioned by
dbSNPrs6864776
ebirs6864776
HLIrs6864776
Exacrs6864776
Varsomers6864776
Maprs6864776
PheGenIrs6864776
hapmaprs6864776
1000 genomesrs6864776
hgdprs6864776
ensemblrs6864776
gopubmedrs6864776
geneviewrs6864776
scholarrs6864776
googlers6864776
pharmgkbrs6864776
gwascentralrs6864776
openSNPrs6864776
23andMers6864776
23andMe allrs6864776
SNP Nexus

SNPshotrs6864776
SNPdbers6864776
MSV3drs6864776
GWAS Ctlgrs6864776
Max Magnitude

[PMID 27640304] Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation.