rs121909580

Orientation

minus

Stabilized

minus

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

Make rs121909580(C;T)

Make rs121909580(T;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

63350572

Gene

CHRNA4

is a	snp
is	mentioned by
dbSNP	rs121909580
dbSNP (classic)	rs121909580
ClinGen	rs121909580
ebi	rs121909580
HLI	rs121909580
Exac	rs121909580
Gnomad	rs121909580
Varsome	rs121909580
LitVar	rs121909580
Map	rs121909580
PheGenI	rs121909580
Biobank	rs121909580
1000 genomes	rs121909580
hgdp	rs121909580
ensembl	rs121909580
geneview	rs121909580
scholar	rs121909580
google	rs121909580
pharmgkb	rs121909580
gwascentral	rs121909580
openSNP	rs121909580
23andMe	rs121909580
SNPshot	rs121909580
SNPdbe	rs121909580
MSV3d	rs121909580
GWAS Ctlg	rs121909580

Max Magnitude

0

OMIM	118504
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121909580(T;T)
Alt	rs121909580(T;T)
Reference	Rs121909580(C;C)
Significance	Pathogenic
Disease	Epilepsy not provided
Variation	info
Gene	CHRNA4
CLNDBN	Epilepsy, nocturnal frontal lobe, type 1 not provided
Reversed	1
HGVS	NC_000020.10:g.61981924G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019050.24, RCV000487099.1,