rs587777557

Orientation

plus

Stabilized

plus

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

Make rs587777557(A;G)

Make rs587777557(G;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

123638288

Gene

SCN3B

is a	snp
is	mentioned by
dbSNP	rs587777557
dbSNP (classic)	rs587777557
ClinGen	rs587777557
ebi	rs587777557
HLI	rs587777557
Exac	rs587777557
Gnomad	rs587777557
Varsome	rs587777557
LitVar	rs587777557
Map	rs587777557
PheGenI	rs587777557
Biobank	rs587777557
1000 genomes	rs587777557
hgdp	rs587777557
ensembl	rs587777557
geneview	rs587777557
scholar	rs587777557
google	rs587777557
pharmgkb	rs587777557
gwascentral	rs587777557
openSNP	rs587777557
23andMe	rs587777557
SNPshot	rs587777557
SNPdbe	rs587777557
MSV3d	rs587777557
GWAS Ctlg	rs587777557

Max Magnitude

0

ClinVar
Risk	rs587777557(G;G)
Alt	rs587777557(G;G)
Reference	Rs587777557(A;A)
Significance	Pathogenic
Disease	Atrial fibrillation
Variation	info
Gene	SCN3B
CLNDBN	Atrial fibrillation, familial, 16
Reversed	0
HGVS	NC_000011.9:g.123508996A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000128814.4,