rs587777556

Orientation

plus

Stabilized

plus

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

Make rs587777556(A;A)

Make rs587777556(A;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

123642502

Gene

SCN3B

is a	snp
is	mentioned by
dbSNP	rs587777556
dbSNP (classic)	rs587777556
ClinGen	rs587777556
ebi	rs587777556
HLI	rs587777556
Exac	rs587777556
Gnomad	rs587777556
Varsome	rs587777556
LitVar	rs587777556
Map	rs587777556
PheGenI	rs587777556
Biobank	rs587777556
1000 genomes	rs587777556
hgdp	rs587777556
ensembl	rs587777556
geneview	rs587777556
scholar	rs587777556
google	rs587777556
pharmgkb	rs587777556
gwascentral	rs587777556
openSNP	rs587777556
23andMe	rs587777556
SNPshot	rs587777556
SNPdbe	rs587777556
MSV3d	rs587777556
GWAS Ctlg	rs587777556

Max Magnitude

0

ClinVar
Risk	rs587777556(A;A) rs587777556(T;T)
Alt	rs587777556(A;A) rs587777556(T;T)
Reference	Rs587777556(G;G)
Significance	Pathogenic
Disease	Atrial fibrillation not specified
Variation	info
Gene	SCN3B
CLNDBN	Atrial fibrillation, familial, 16 not specified
Reversed	0
HGVS	NC_000011.9:g.123513210G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000128813.4, RCV000480040.1,