rs17121819

Orientation

minus

Stabilized

minus

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

Make rs17121819(C;T)

Make rs17121819(T;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

118168740

Gene

SCN2B

is a	snp
is	mentioned by
dbSNP	rs17121819
dbSNP (classic)	rs17121819
ClinGen	rs17121819
ebi	rs17121819
HLI	rs17121819
Exac	rs17121819
Gnomad	rs17121819
Varsome	rs17121819
LitVar	rs17121819
Map	rs17121819
PheGenI	rs17121819
Biobank	rs17121819
1000 genomes	rs17121819
hgdp	rs17121819
ensembl	rs17121819
geneview	rs17121819
scholar	rs17121819
google	rs17121819
pharmgkb	rs17121819
gwascentral	rs17121819
openSNP	rs17121819
23andMe	rs17121819
SNPshot	rs17121819
SNPdbe	rs17121819
MSV3d	rs17121819
GWAS Ctlg	rs17121819

Max Magnitude

0

ClinVar
Risk	rs17121819(T;T)
Alt	rs17121819(T;T)
Reference	Rs17121819(C;C)
Significance	Pathogenic
Disease	Atrial fibrillation not specified
Variation	info
Gene	SCN2B
CLNDBN	Atrial fibrillation, familial, 14 not specified
Reversed	1
HGVS	NC_000011.9:g.118039455G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000054539.2, RCV000483016.1,