rs104893712

Orientation

plus

Stabilized

plus

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

Make rs104893712(A;A)

Make rs104893712(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

122283764

Gene

CASR

is a	snp
is	mentioned by
dbSNP	rs104893712
dbSNP (classic)	rs104893712
ClinGen	rs104893712
ebi	rs104893712
HLI	rs104893712
Exac	rs104893712
Gnomad	rs104893712
Varsome	rs104893712
LitVar	rs104893712
Map	rs104893712
PheGenI	rs104893712
Biobank	rs104893712
1000 genomes	rs104893712
hgdp	rs104893712
ensembl	rs104893712
geneview	rs104893712
scholar	rs104893712
google	rs104893712
pharmgkb	rs104893712
gwascentral	rs104893712
openSNP	rs104893712
23andMe	rs104893712
SNPshot	rs104893712
SNPdbe	rs104893712
MSV3d	rs104893712
GWAS Ctlg	rs104893712

Max Magnitude

0

OMIM	601199
Desc
Variant	0041
Related	also

ClinVar
Risk	rs104893712(A;A)
Alt	rs104893712(A;A)
Reference	Rs104893712(G;G)
Significance	Pathogenic
Disease	Hypocalcemia not provided
Variation	info
Gene	CASR
CLNDBN	Hypocalcemia, autosomal dominant 1 not provided
Reversed	0
HGVS	NC_000003.11:g.122002611G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008855.5, RCV000414467.1,