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rs6013897

From SNPedia

Orientationplus
Stabilizedplus
Make rs6013897(A;A)
Make rs6013897(A;T)
Make rs6013897(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position54125940
is asnp
is mentioned by
dbSNPrs6013897
ebirs6013897
HLIrs6013897
Exacrs6013897
Varsomers6013897
Maprs6013897
PheGenIrs6013897
hapmaprs6013897
1000 genomesrs6013897
hgdprs6013897
ensemblrs6013897
gopubmedrs6013897
geneviewrs6013897
scholarrs6013897
googlers6013897
pharmgkbrs6013897
gwascentralrs6013897
openSNPrs6013897
23andMers6013897
23andMe allrs6013897
SNP Nexus

SNPshotrs6013897
SNPdbers6013897
MSV3drs6013897
GWAS Ctlgrs6013897
GMAF0.2332
Max Magnitude
? (A;A) (A;T) (T;T) 28
[PMID 22629401OA-icon.png] Evaluation of Genetic Markers as Instruments for Mendelian Randomization Studies on Vitamin D

[PMID 22649517OA-icon.png] Polymorphisms related to the serum 25-hydroxyvitamin d level and risk of myocardial infarction, diabetes, cancer and mortality. The tromsø study


[PMID 20541252OA-icon.png] Common genetic determinants of vitamin D insufficiency: a genome-wide association study.


[PMID 22701574OA-icon.png] Instrumental variable estimation of the causal effect of plasma 25-hydroxy-vitamin D on colorectal cancer risk: a mendelian randomization analysis


[PMID 23377224OA-icon.png] Genetic Variation in the Vitamin D Pathway in Relation to Risk of Prostate Cancer - Results from Breast and Prostate Cancer Cohort Consortium (BPC3)


[PMID 23924835] Genetic variant in vitamin D binding protein is associated with serum 25-hydroxyvitamin D and vitamin D insufficiency in southern Chinese


[PMID 22740028OA-icon.png] An exploratory analysis of common genetic variants in the vitamin D pathway including genome-wide associated variants in relation to glioma risk and outcome.


[PMID 26448018] Variants in Vitamin D Binding Protein Gene Are Associated With Gestational Diabetes Mellitus


[PMID 27813049] Genetic Expression Profile of Vitamin D Metabolizing Enzymes in the First Trimester.