rs121909795

Orientation

minus

Stabilized

minus

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

Make rs121909795(C;T)

Make rs121909795(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

47857512

Gene

VDR

is a	snp
is	mentioned by
dbSNP	rs121909795
dbSNP (classic)	rs121909795
ClinGen	rs121909795
ebi	rs121909795
HLI	rs121909795
Exac	rs121909795
Gnomad	rs121909795
Varsome	rs121909795
LitVar	rs121909795
Map	rs121909795
PheGenI	rs121909795
Biobank	rs121909795
1000 genomes	rs121909795
hgdp	rs121909795
ensembl	rs121909795
geneview	rs121909795
scholar	rs121909795
google	rs121909795
pharmgkb	rs121909795
gwascentral	rs121909795
openSNP	rs121909795
23andMe	rs121909795
SNPshot	rs121909795
SNPdbe	rs121909795
MSV3d	rs121909795
GWAS Ctlg	rs121909795

Max Magnitude

0

OMIM	601769
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121909795(T;T)
Alt	rs121909795(T;T)
Reference	Rs121909795(C;C)
Significance	Pathogenic
Disease	Vitamin D-dependent rickets
Variation	info
Gene	VDR
CLNDBN	Vitamin D-dependent rickets, type 2
Reversed	1
HGVS	NC_000012.11:g.48251295G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008192.4,