rs121909261

Orientation

plus

Stabilized

plus

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

Make rs121909261(G;T)

Make rs121909261(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

122283997

Gene

CASR

is a	snp
is	mentioned by
dbSNP	rs121909261
dbSNP (classic)	rs121909261
ClinGen	rs121909261
ebi	rs121909261
HLI	rs121909261
Exac	rs121909261
Gnomad	rs121909261
Varsome	rs121909261
LitVar	rs121909261
Map	rs121909261
PheGenI	rs121909261
Biobank	rs121909261
1000 genomes	rs121909261
hgdp	rs121909261
ensembl	rs121909261
geneview	rs121909261
scholar	rs121909261
google	rs121909261
pharmgkb	rs121909261
gwascentral	rs121909261
openSNP	rs121909261
23andMe	rs121909261
SNPshot	rs121909261
SNPdbe	rs121909261
MSV3d	rs121909261
GWAS Ctlg	rs121909261

Max Magnitude

0

OMIM	601199
Desc
Variant	0009
Related	also

ClinVar
Risk	rs121909261(T;T)
Alt	rs121909261(T;T)
Reference	Rs121909261(G;G)
Significance	Pathogenic
Disease	Hypocalcemia
Variation	info
Gene	CASR
CLNDBN	Hypocalcemia, autosomal dominant 1
Reversed	0
HGVS	NC_000003.11:g.122002844G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008821.3,