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rs4665972

From SNPedia

Orientationplus
Stabilizedplus
Make rs4665972(C;C)
Make rs4665972(C;T)
Make rs4665972(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position27375230
GeneSNX17
is asnp
is mentioned by
dbSNPrs4665972
dbSNP (classic)rs4665972
ClinGenrs4665972
ebirs4665972
HLIrs4665972
Exacrs4665972
Gnomadrs4665972
Varsomers4665972
LitVarrs4665972
Maprs4665972
PheGenIrs4665972
Biobankrs4665972
1000 genomesrs4665972
hgdprs4665972
ensemblrs4665972
geneviewrs4665972
scholarrs4665972
googlers4665972
pharmgkbrs4665972
gwascentralrs4665972
openSNPrs4665972
23andMers4665972
SNPshotrs4665972
SNPdbers4665972
MSV3drs4665972
GWAS Ctlgrs4665972
GMAF0.3806
Max Magnitude0
GWAS snp
PMID [PMID 22747683OA-icon.png]
Trait Breast size
Title Genetic variants associated with breast size also influence breast cancer risk.
Risk Allele T
P-val 1E-6
Odds Ratio .08 [0.047-0.113] cup size increase
GWAS snp
PMID [PMID 23726366OA-icon.png]
Trait Triglycerides
Title Genome-wide Characterization of Shared and Distinct Genetic Components that Influence Blood Lipid Levels in Ethnically Diverse Human Populations.
Risk Allele T
P-val 1E-8
Odds Ratio .07 [NR] unit increase