rs587777560

Orientation

plus

Stabilized

minus

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

Make rs587777560(G;G)

Make rs587777560(G;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

118141304

Gene

SCN4B

is a	snp
is	mentioned by
dbSNP	rs587777560
dbSNP (classic)	rs587777560
ClinGen	rs587777560
ebi	rs587777560
HLI	rs587777560
Exac	rs587777560
Gnomad	rs587777560
Varsome	rs587777560
LitVar	rs587777560
Map	rs587777560
PheGenI	rs587777560
Biobank	rs587777560
1000 genomes	rs587777560
hgdp	rs587777560
ensembl	rs587777560
geneview	rs587777560
scholar	rs587777560
google	rs587777560
pharmgkb	rs587777560
gwascentral	rs587777560
openSNP	rs587777560
23andMe	rs587777560
SNPshot	rs587777560
SNPdbe	rs587777560
MSV3d	rs587777560
GWAS Ctlg	rs587777560

Max Magnitude

0

ClinVar
Risk	rs587777560(G;G) Rs587777560(T;T)
Alt	rs587777560(G;G) Rs587777560(T;T)
Reference	Rs587777560(A;A)
Significance	Pathogenic
Disease	Atrial fibrillation
Variation	info
Gene	SCN4B
CLNDBN	Atrial fibrillation, familial, 17
Reversed	1
HGVS	NC_000011.9:g.118012019T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000128817.2,