rs104893702

Orientation

plus

Stabilized

plus

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

Make rs104893702(A;C)

Make rs104893702(C;C)

Reference

GRCh38 38.1/141

Chromosome

3

Position

122254330

Gene

CASR

is a	snp
is	mentioned by
dbSNP	rs104893702
dbSNP (classic)	rs104893702
ClinGen	rs104893702
ebi	rs104893702
HLI	rs104893702
Exac	rs104893702
Gnomad	rs104893702
Varsome	rs104893702
LitVar	rs104893702
Map	rs104893702
PheGenI	rs104893702
Biobank	rs104893702
1000 genomes	rs104893702
hgdp	rs104893702
ensembl	rs104893702
geneview	rs104893702
scholar	rs104893702
google	rs104893702
pharmgkb	rs104893702
gwascentral	rs104893702
openSNP	rs104893702
23andMe	rs104893702
SNPshot	rs104893702
SNPdbe	rs104893702
MSV3d	rs104893702
GWAS Ctlg	rs104893702

Max Magnitude

0

OMIM	601199
Desc
Variant	0028
Related	also

ClinVar
Risk	rs104893702(C;C)
Alt	rs104893702(C;C)
Reference	Rs104893702(A;A)
Significance	Pathogenic
Disease	Hypocalcemia
Variation	info
Gene	CASR
CLNDBN	Hypocalcemia, autosomal dominant 1
Reversed	0
HGVS	NC_000003.11:g.121973177A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008839.5,