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rs17879735

From SNPedia

Merged intors7975232
Orientationplus
Make rs17879735(A;A)
Make rs17879735(A;C)
Make rs17879735(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position47845054
GeneLOC105369749, VDR
is asnp
is mentioned by
dbSNPrs17879735
ebirs17879735
HLIrs17879735
Exacrs17879735
Varsomers17879735
Maprs17879735
PheGenIrs17879735
hapmaprs17879735
1000 genomesrs17879735
hgdprs17879735
ensemblrs17879735
gopubmedrs17879735
geneviewrs17879735
scholarrs17879735
googlers17879735
pharmgkbrs17879735
gwascentralrs17879735
openSNPrs17879735
23andMers17879735
23andMe allrs17879735
SNP Nexus

SNPshotrs17879735
SNPdbers17879735
MSV3drs17879735
GWAS Ctlgrs17879735
StatusMerged into rs7975232
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 27446548] Association between the vitamin D receptor gene polymorphism and osteoporosis.