rs1057521095

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs1057521095(C;T)

Make rs1057521095(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

47845003

Gene

VDR

is a	snp
is	mentioned by
dbSNP	rs1057521095
dbSNP (classic)	rs1057521095
ClinGen	rs1057521095
ebi	rs1057521095
HLI	rs1057521095
Exac	rs1057521095
Gnomad	rs1057521095
Varsome	rs1057521095
LitVar	rs1057521095
Map	rs1057521095
PheGenI	rs1057521095
Biobank	rs1057521095
1000 genomes	rs1057521095
hgdp	rs1057521095
ensembl	rs1057521095
geneview	rs1057521095
scholar	rs1057521095
google	rs1057521095
pharmgkb	rs1057521095
gwascentral	rs1057521095
openSNP	rs1057521095
23andMe	rs1057521095
SNPshot	rs1057521095
SNPdbe	rs1057521095
MSV3d	rs1057521095
GWAS Ctlg	rs1057521095

Max Magnitude

0

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,