Have questions? Visit https://www.reddit.com/r/SNPedia

rs2762934

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2762934(A;A)
Make rs2762934(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position54154722
GeneCYP24A1
is asnp
is mentioned by
dbSNPrs2762934
dbSNP (classic)rs2762934
ClinGenrs2762934
ebirs2762934
HLIrs2762934
Exacrs2762934
Gnomadrs2762934
Varsomers2762934
LitVarrs2762934
Maprs2762934
PheGenIrs2762934
Biobankrs2762934
1000 genomesrs2762934
hgdprs2762934
ensemblrs2762934
geneviewrs2762934
scholarrs2762934
googlers2762934
pharmgkbrs2762934
gwascentralrs2762934
openSNPrs2762934
23andMers2762934
SNPshotrs2762934
SNPdbers2762934
MSV3drs2762934
GWAS Ctlgrs2762934
GMAF0.169
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 23393347OA-icon.png] Sunlight, Polymorphisms of Vitamin D-related Genes and Risk of Breast Cancer


[PMID 21819409OA-icon.png] Gene-vitamin D interactions on food sensitization: a prospective birth cohort study.


ClinVar
Risk rs2762934(A;A)
Alt rs2762934(A;A)
Reference Rs2762934(G;G)
Significance Non-pathogenic
Disease Infantile hypercalcemia
Variation info
Gene CYP24A1
CLNDBN Infantile hypercalcemia
Reversed 0
HGVS NC_000020.10:g.52771261G>A
CLNSRC
CLNACC RCV000314102.1,