rs121909269

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs121909269(A;A)

Make rs121909269(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

122284647

Gene

CASR

is a	snp
is	mentioned by
dbSNP	rs121909269
dbSNP (classic)	rs121909269
ClinGen	rs121909269
ebi	rs121909269
HLI	rs121909269
Exac	rs121909269
Gnomad	rs121909269
Varsome	rs121909269
LitVar	rs121909269
Map	rs121909269
PheGenI	rs121909269
Biobank	rs121909269
1000 genomes	rs121909269
hgdp	rs121909269
ensembl	rs121909269
geneview	rs121909269
scholar	rs121909269
google	rs121909269
pharmgkb	rs121909269
gwascentral	rs121909269
openSNP	rs121909269
23andMe	rs121909269
SNPshot	rs121909269
SNPdbe	rs121909269
MSV3d	rs121909269
GWAS Ctlg	rs121909269

Max Magnitude

0

OMIM	601199
Desc
Variant	0050
Related	also

ClinVar
Risk	rs121909269(A;A)
Alt	rs121909269(A;A)
Reference	Rs121909269(G;G)
Significance	Other
Disease	Epilepsy
Variation	info
Gene	CASR
CLNDBN	Epilepsy, idiopathic generalized 8
Reversed	0
HGVS	NC_000003.11:g.122003494G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008864.4,