rs587777558

Orientation

plus

Stabilized

minus

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

Make rs587777558(C;T)

Make rs587777558(T;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

123653785

Gene	LOC105369543, SCN3B

is a	snp
is	mentioned by
dbSNP	rs587777558
dbSNP (classic)	rs587777558
ClinGen	rs587777558
ebi	rs587777558
HLI	rs587777558
Exac	rs587777558
Gnomad	rs587777558
Varsome	rs587777558
LitVar	rs587777558
Map	rs587777558
PheGenI	rs587777558
Biobank	rs587777558
1000 genomes	rs587777558
hgdp	rs587777558
ensembl	rs587777558
geneview	rs587777558
scholar	rs587777558
google	rs587777558
pharmgkb	rs587777558
gwascentral	rs587777558
openSNP	rs587777558
23andMe	rs587777558
SNPshot	rs587777558
SNPdbe	rs587777558
MSV3d	rs587777558
GWAS Ctlg	rs587777558

Max Magnitude

0

ClinVar
Risk	Rs587777558(C;C) rs587777558(T;T)
Alt	Rs587777558(C;C) rs587777558(T;T)
Reference	Rs587777558(G;G)
Significance	Pathogenic
Disease	Atrial fibrillation
Variation	info
Gene	SCN3B
CLNDBN	Atrial fibrillation, familial, 16
Reversed	1
HGVS	NC_000011.9:g.123524493C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000128815.4,