rs16969925

Orientation

plus

Stabilized

plus

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

Make rs16969925(A;A)

Make rs16969925(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

35033545

Gene

SCN1B

is a	snp
is	mentioned by
dbSNP	rs16969925
dbSNP (classic)	rs16969925
ClinGen	rs16969925
ebi	rs16969925
HLI	rs16969925
Exac	rs16969925
Gnomad	rs16969925
Varsome	rs16969925
LitVar	rs16969925
Map	rs16969925
PheGenI	rs16969925
Biobank	rs16969925
1000 genomes	rs16969925
hgdp	rs16969925
ensembl	rs16969925
geneview	rs16969925
scholar	rs16969925
google	rs16969925
pharmgkb	rs16969925
gwascentral	rs16969925
openSNP	rs16969925
23andMe	rs16969925
SNPshot	rs16969925
SNPdbe	rs16969925
MSV3d	rs16969925
GWAS Ctlg	rs16969925

Max Magnitude

0

ClinVar
Risk	rs16969925(A;A)
Alt	rs16969925(A;A)
Reference	Rs16969925(G;G)
Significance	Pathogenic
Disease	Atrial fibrillation not provided
Variation	info
Gene	SCN1B
CLNDBN	Atrial fibrillation, familial, 13 not provided
Reversed	0
HGVS	NC_000019.9:g.35524449G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000054537.2, RCV000485749.1,