rs121909264

Orientation

plus

Stabilized

plus

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

Make rs121909264(A;A)

Make rs121909264(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

122257323

Gene

CASR

is a	snp
is	mentioned by
dbSNP	rs121909264
dbSNP (classic)	rs121909264
ClinGen	rs121909264
ebi	rs121909264
HLI	rs121909264
Exac	rs121909264
Gnomad	rs121909264
Varsome	rs121909264
LitVar	rs121909264
Map	rs121909264
PheGenI	rs121909264
Biobank	rs121909264
1000 genomes	rs121909264
hgdp	rs121909264
ensembl	rs121909264
geneview	rs121909264
scholar	rs121909264
google	rs121909264
pharmgkb	rs121909264
gwascentral	rs121909264
openSNP	rs121909264
23andMe	rs121909264
SNPshot	rs121909264
SNPdbe	rs121909264
MSV3d	rs121909264
GWAS Ctlg	rs121909264

Max Magnitude

0

OMIM	601199
Desc
Variant	0024
Related	also

ClinVar
Risk	rs121909264(A;A)
Alt	rs121909264(A;A)
Reference	Rs121909264(G;G)
Significance	Pathogenic
Disease	Hypocalciuric hypercalcemia
Variation	info
Gene	CASR
CLNDBN	Hypocalciuric hypercalcemia, familial, type 1
Reversed	0
HGVS	NC_000003.11:g.121976170G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008835.6,