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rs7716600

From SNPedia

Orientationplus
Stabilizedplus
Make rs7716600(A;A)
Make rs7716600(A;C)
Make rs7716600(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position44874903
is asnp
is mentioned by
dbSNPrs7716600
ebirs7716600
HLIrs7716600
Exacrs7716600
Varsomers7716600
Maprs7716600
PheGenIrs7716600
hapmaprs7716600
1000 genomesrs7716600
hgdprs7716600
ensemblrs7716600
gopubmedrs7716600
geneviewrs7716600
scholarrs7716600
googlers7716600
pharmgkbrs7716600
gwascentralrs7716600
openSNPrs7716600
23andMers7716600
23andMe allrs7716600
SNP Nexus

SNPshotrs7716600
SNPdbers7716600
MSV3drs7716600
GWAS Ctlgrs7716600
GMAF0.2713
Max Magnitude
? (A;A) (A;C) (C;C) 28
Perhaps this paper discusses this snp, however since it is on chromosome 5, it is not one of the 2 discussed in the abstract. [PMID 19330030OA-icon.png] nature
GWAS snp
PMID [PMID 20872241]
Trait
Title A combined analysis of genome-wide association studies in breast cancer
Risk Allele A
P-val 7E-7
Odds Ratio 1.24 [1.14-1.34]


[PMID 21445572] Genetic polymorphisms and breast cancer risk: evidence from meta-analyses, pooled analyses, and genome-wide association studies


[PMID 22452962OA-icon.png] A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study


[PMID 20237344OA-icon.png] Performance of common genetic variants in breast-cancer risk models.


[PMID 24388359OA-icon.png] The 5p12 breast cancer susceptibility locus affects MRPS30 expression in estrogen-receptor positive tumors