rs1805032

Orientation

minus

Stabilized

minus

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

Make rs1805032(C;T)

Make rs1805032(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

151839238

Gene

CACNB4

is a	snp
is	mentioned by
dbSNP	rs1805032
dbSNP (classic)	rs1805032
ClinGen	rs1805032
ebi	rs1805032
HLI	rs1805032
Exac	rs1805032
Gnomad	rs1805032
Varsome	rs1805032
LitVar	rs1805032
Map	rs1805032
PheGenI	rs1805032
Biobank	rs1805032
1000 genomes	rs1805032
hgdp	rs1805032
ensembl	rs1805032
geneview	rs1805032
scholar	rs1805032
google	rs1805032
pharmgkb	rs1805032
gwascentral	rs1805032
openSNP	rs1805032
23andMe	rs1805032
SNPshot	rs1805032
SNPdbe	rs1805032
MSV3d	rs1805032
GWAS Ctlg	rs1805032

Max Magnitude

0

OMIM	601949
Desc
Variant	0001
Related	also

ClinVar
Risk	rs1805032(T;T)
Alt	rs1805032(T;T)
Reference	Rs1805032(C;C)
Significance	Other
Disease	Epilepsy
Variation	info
Gene	CACNB4
CLNDBN	Epilepsy, juvenile myoclonic 6
Reversed	1
HGVS	NC_000002.11:g.152695752G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008045.2,