rs587777559

Orientation

plus

Stabilized

minus

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

Make rs587777559(A;C)

Make rs587777559(C;C)

Reference

GRCh38 38.1/142

Chromosome

11

Position

118141315

Gene

SCN4B

is a	snp
is	mentioned by
dbSNP	rs587777559
dbSNP (classic)	rs587777559
ClinGen	rs587777559
ebi	rs587777559
HLI	rs587777559
Exac	rs587777559
Gnomad	rs587777559
Varsome	rs587777559
LitVar	rs587777559
Map	rs587777559
PheGenI	rs587777559
Biobank	rs587777559
1000 genomes	rs587777559
hgdp	rs587777559
ensembl	rs587777559
geneview	rs587777559
scholar	rs587777559
google	rs587777559
pharmgkb	rs587777559
gwascentral	rs587777559
openSNP	rs587777559
23andMe	rs587777559
SNPshot	rs587777559
SNPdbe	rs587777559
MSV3d	rs587777559
GWAS Ctlg	rs587777559

Max Magnitude

0

ClinVar
Risk	Rs587777559(A;A) rs587777559(C;C)
Alt	Rs587777559(A;A) rs587777559(C;C)
Reference	Rs587777559(T;T)
Significance	Pathogenic
Disease	Atrial fibrillation
Variation	info
Gene	SCN4B
CLNDBN	Atrial fibrillation, familial, 17
Reversed	1
HGVS	NC_000011.9:g.118012030A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000128816.2,