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rs10484919

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs10484919(C;T)
Make rs10484919(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position151653287
is asnp
is mentioned by
dbSNPrs10484919
ebirs10484919
HLIrs10484919
Exacrs10484919
Varsomers10484919
Maprs10484919
PheGenIrs10484919
hapmaprs10484919
1000 genomesrs10484919
hgdprs10484919
ensemblrs10484919
gopubmedrs10484919
geneviewrs10484919
scholarrs10484919
googlers10484919
pharmgkbrs10484919
gwascentralrs10484919
openSNPrs10484919
23andMers10484919
23andMe allrs10484919
SNP Nexus

SNPshotrs10484919
SNPdbers10484919
MSV3drs10484919
GWAS Ctlgrs10484919
GMAF0.186
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 21528353] Genetic variants of 6q25 and breast cancer susceptibility: a two-stage fine mapping study in a Chinese population