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rs2580520

From SNPedia

Orientationplus
Stabilizedplus
Make rs2580520(C;C)
Make rs2580520(C;G)
Make rs2580520(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position121370191
GeneSRGAP2-AS1, SRGAP2C
is asnp
is mentioned by
dbSNPrs2580520
ebirs2580520
HLIrs2580520
Exacrs2580520
Varsomers2580520
Maprs2580520
PheGenIrs2580520
hapmaprs2580520
1000 genomesrs2580520
hgdprs2580520
ensemblrs2580520
gopubmedrs2580520
geneviewrs2580520
scholarrs2580520
googlers2580520
pharmgkbrs2580520
gwascentralrs2580520
openSNPrs2580520
23andMers2580520
23andMe allrs2580520
SNP Nexus

SNPshotrs2580520
SNPdbers2580520
MSV3drs2580520
GWAS Ctlgrs2580520
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 21738711OA-icon.png]

Genetic variants at 1p11.2 and breast cancer risk: a two-stage study in Chinese women.

one SNP (rs2580520) located at a predicted enhancer region of SRGAP2 was consistently associated with a significantly increased risk of breast cancer in a recessive genetic model [Odds Ratio (OR)  =  1.66, 95% confidence interval (CI)  =  1.16-2.36 for stage 2 samples; OR  =  1.51, 95% CI  =  1.16-1.97 for combined samples, respectively].