rs74315291

Orientation

plus

Stabilized

plus

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

Make rs74315291(C;C)

Make rs74315291(C;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

154571682

Gene

CHRNB2

is a	snp
is	mentioned by
dbSNP	rs74315291
dbSNP (classic)	rs74315291
ClinGen	rs74315291
ebi	rs74315291
HLI	rs74315291
Exac	rs74315291
Gnomad	rs74315291
Varsome	rs74315291
LitVar	rs74315291
Map	rs74315291
PheGenI	rs74315291
Biobank	rs74315291
1000 genomes	rs74315291
hgdp	rs74315291
ensembl	rs74315291
geneview	rs74315291
scholar	rs74315291
google	rs74315291
pharmgkb	rs74315291
gwascentral	rs74315291
openSNP	rs74315291
23andMe	rs74315291
SNPshot	rs74315291
SNPdbe	rs74315291
MSV3d	rs74315291
GWAS Ctlg	rs74315291

Max Magnitude

0

OMIM	118507
Desc
Variant	0001
Related	also

OMIM	118507
Desc
Variant	0002
Related	also

ClinVar
Risk	rs74315291(A;A) rs74315291(C;C) rs74315291(T;T)
Alt	rs74315291(A;A) rs74315291(C;C) rs74315291(T;T)
Reference	Rs74315291(G;G)
Significance	Pathogenic
Disease	Epilepsy
Variation	info
Gene	CHRNB2
CLNDBN	Epilepsy, nocturnal frontal lobe, type 3
Reversed	0
HGVS	NC_000001.10:g.154544158G>A; NC_000001.10:g.154544158G>C; NC_000001.10:g.154544158G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019048.28, RCV000019047.28, RCV000033930.2,