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rs1790349

From SNPedia

Orientationminus
Stabilizedminus
Make rs1790349(A;A)
Make rs1790349(A;G)
Make rs1790349(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position71431304
is asnp
is mentioned by
dbSNPrs1790349
dbSNP (classic)rs1790349
ClinGenrs1790349
ebirs1790349
HLIrs1790349
Exacrs1790349
Gnomadrs1790349
Varsomers1790349
LitVarrs1790349
Maprs1790349
PheGenIrs1790349
Biobankrs1790349
1000 genomesrs1790349
hgdprs1790349
ensemblrs1790349
geneviewrs1790349
scholarrs1790349
googlers1790349
pharmgkbrs1790349
gwascentralrs1790349
openSNPrs1790349
23andMers1790349
SNPshotrs1790349
SNPdbers1790349
MSV3drs1790349
GWAS Ctlgrs1790349
GMAF0.2241
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 23505139] An analysis of the association between the vitamin D pathway and serum 25-hydroxyvitamin D levels in a healthy Chinese population


[PMID 20418485OA-icon.png] Genome-wide association study of circulating vitamin D levels.


[PMID 21972121] Associations between common variants in GC and DHCR7/NADSYN1 and vitamin D concentration in Chinese Hans.