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rs1057521095

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521095(C;T)
Make rs1057521095(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position47845003
GeneVDR
is asnp
is mentioned by
dbSNPrs1057521095
dbSNP (old)rs1057521095
ClinGenrs1057521095
ebirs1057521095
HLIrs1057521095
Exacrs1057521095
Gnomadrs1057521095
Varsomers1057521095
Maprs1057521095
PheGenIrs1057521095
Biobankrs1057521095
1000 genomesrs1057521095
hgdprs1057521095
ensemblrs1057521095
gopubmedrs1057521095
geneviewrs1057521095
scholarrs1057521095
googlers1057521095
pharmgkbrs1057521095
gwascentralrs1057521095
openSNPrs1057521095
23andMers1057521095
23andMe allrs1057521095
SNPshotrs1057521095
SNPdbers1057521095
MSV3drs1057521095
GWAS Ctlgrs1057521095
Max Magnitude0
ClinVar
Risk rs1057521095(T;T)
Alt rs1057521095(T;T)
Reference Rs1057521095(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene VDR
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.48238786G>A
CLNSRC
CLNACC RCV000421461.1,