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rs10494836

From SNPedia

Orientationplus
Stabilizedplus
Make rs10494836(C;C)
Make rs10494836(C;T)
Make rs10494836(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position202727750
GeneKDM5B
is asnp
is mentioned by
dbSNPrs10494836
ebirs10494836
HLIrs10494836
Exacrs10494836
Varsomers10494836
Maprs10494836
PheGenIrs10494836
hapmaprs10494836
1000 genomesrs10494836
hgdprs10494836
ensemblrs10494836
gopubmedrs10494836
geneviewrs10494836
scholarrs10494836
googlers10494836
pharmgkbrs10494836
gwascentralrs10494836
openSNPrs10494836
23andMers10494836
23andMe allrs10494836
SNP Nexus

SNPshotrs10494836
SNPdbers10494836
MSV3drs10494836
GWAS Ctlgrs10494836
GMAF0.1107
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 23188672] Genetic variation in a hsa-let-7 binding site in RAD52 is associated with breast cancer susceptibility