rs72544145

Orientation

minus

Stabilized

minus

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

Make rs72544145(A;A)

Make rs72544145(A;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

118168739

Gene

SCN2B

is a	snp
is	mentioned by
dbSNP	rs72544145
dbSNP (classic)	rs72544145
ClinGen	rs72544145
ebi	rs72544145
HLI	rs72544145
Exac	rs72544145
Gnomad	rs72544145
Varsome	rs72544145
LitVar	rs72544145
Map	rs72544145
PheGenI	rs72544145
Biobank	rs72544145
1000 genomes	rs72544145
hgdp	rs72544145
ensembl	rs72544145
geneview	rs72544145
scholar	rs72544145
google	rs72544145
pharmgkb	rs72544145
gwascentral	rs72544145
openSNP	rs72544145
23andMe	rs72544145
SNPshot	rs72544145
SNPdbe	rs72544145
MSV3d	rs72544145
GWAS Ctlg	rs72544145

Max Magnitude

0

ClinVar
Risk	rs72544145(A;A)
Alt	rs72544145(A;A)
Reference	Rs72544145(G;G)
Significance	Pathogenic
Disease	Atrial fibrillation
Variation	info
Gene	SCN2B
CLNDBN	Atrial fibrillation, familial, 14
Reversed	1
HGVS	NC_000011.9:g.118039454C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000054540.2,