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

rs777947329

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs777947329(A;A)
Make rs777947329(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position54159075
GeneCYP24A1
is asnp
is mentioned by
dbSNPrs777947329
ebirs777947329
HLIrs777947329
Exacrs777947329
Varsomers777947329
Maprs777947329
PheGenIrs777947329
hapmaprs777947329
1000 genomesrs777947329
hgdprs777947329
ensemblrs777947329
gopubmedrs777947329
geneviewrs777947329
scholarrs777947329
googlers777947329
pharmgkbrs777947329
gwascentralrs777947329
openSNPrs777947329
23andMers777947329
23andMe allrs777947329
SNP Nexus

SNPshotrs777947329
SNPdbers777947329
MSV3drs777947329
GWAS Ctlgrs777947329
Max Magnitude0
ClinVar
Risk rs777947329(A;A)
Alt rs777947329(A;A)
Reference rs777947329(G;G)
Significance Probable-Pathogenic
Disease Idiopathic hypercalcemia of infancy
Variation info
Gene CYP24A1
CLNDBN Idiopathic hypercalcemia of infancy
Reversed 0
HGVS NC_000020.10:g.52775614G>A
CLNSRC
CLNACC RCV000190576.1,