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rs3755967

From SNPedia

Orientationminus
Stabilizedminus
Make rs3755967(A;A)
Make rs3755967(A;G)
Make rs3755967(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position71743681
GeneGC
is asnp
is mentioned by
dbSNPrs3755967
dbSNP (classic)rs3755967
ClinGenrs3755967
ebirs3755967
HLIrs3755967
Exacrs3755967
Gnomadrs3755967
Varsomers3755967
LitVarrs3755967
Maprs3755967
PheGenIrs3755967
Biobankrs3755967
1000 genomesrs3755967
hgdprs3755967
ensemblrs3755967
geneviewrs3755967
scholarrs3755967
googlers3755967
pharmgkbrs3755967
gwascentralrs3755967
openSNPrs3755967
23andMers3755967
SNPshotrs3755967
SNPdbers3755967
MSV3drs3755967
GWAS Ctlgrs3755967
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 25174667] Environmental and Genetic Determinants of Vitamin D Insufficiency in 12-month-old Infants


[PMID 27282160] GC and VDR SNPs and Vitamin D Levels in Parkinson's Disease: The Relevance to Clinical Features.


[PMID 30716477OA-icon.png] No Association Between Vitamin D Status and Risk of Barrett's Esophagus or Esophageal Adenocarcinoma-a Mendelian Randomization Study.