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rs2296239

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2296239(C;T)
Make rs2296239(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position54158989
GeneCYP24A1
is asnp
is mentioned by
dbSNPrs2296239
dbSNP (old)rs2296239
ClinGenrs2296239
ebirs2296239
HLIrs2296239
Exacrs2296239
Gnomadrs2296239
Varsomers2296239
Maprs2296239
PheGenIrs2296239
Biobankrs2296239
1000 genomesrs2296239
hgdprs2296239
ensemblrs2296239
gopubmedrs2296239
geneviewrs2296239
scholarrs2296239
googlers2296239
pharmgkbrs2296239
gwascentralrs2296239
openSNPrs2296239
23andMers2296239
23andMe allrs2296239
SNP Nexus

SNPshotrs2296239
SNPdbers2296239
MSV3drs2296239
GWAS Ctlgrs2296239
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 23381556OA-icon.png] Genetic association analysis of vitamin D pathway with obesity traits


ClinVar
Risk rs2296239(T;T)
Alt rs2296239(T;T)
Reference Rs2296239(C;C)
Significance Non-pathogenic
Disease Infantile hypercalcemia
Variation info
Gene CYP24A1
CLNDBN Infantile hypercalcemia
Reversed 0
HGVS NC_000020.10:g.52775528C>T
CLNSRC
CLNACC RCV000262895.1,