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rs7999699

From SNPedia

Orientationplus
Stabilizedplus
Make rs7999699(A;A)
Make rs7999699(A;G)
Make rs7999699(G;G)
ReferenceGRCh38 38.1/142
Chromosome13
Position47795595
is asnp
is mentioned by
dbSNPrs7999699
ebirs7999699
HLIrs7999699
Exacrs7999699
Varsomers7999699
Maprs7999699
PheGenIrs7999699
hapmaprs7999699
1000 genomesrs7999699
hgdprs7999699
ensemblrs7999699
gopubmedrs7999699
geneviewrs7999699
scholarrs7999699
googlers7999699
pharmgkbrs7999699
gwascentralrs7999699
openSNPrs7999699
23andMers7999699
23andMe allrs7999699
SNP Nexus

SNPshotrs7999699
SNPdbers7999699
MSV3drs7999699
GWAS Ctlgrs7999699
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 24743840OA-icon.png]
Trait Colorectal cancer (diet interaction)
Title Genome-wide diet-gene interaction analyses for risk of colorectal cancer.
Risk Allele
P-val 3E-6
Odds Ratio 1.32 [1.18-1.47]