rs193922728

Orientation

plus

Stabilized

plus

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

Make rs193922728(A;A)

Make rs193922728(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

35034042

Gene

SCN1B

is a	snp
is	mentioned by
dbSNP	rs193922728
dbSNP (classic)	rs193922728
ClinGen	rs193922728
ebi	rs193922728
HLI	rs193922728
Exac	rs193922728
Gnomad	rs193922728
Varsome	rs193922728
LitVar	rs193922728
Map	rs193922728
PheGenI	rs193922728
Biobank	rs193922728
1000 genomes	rs193922728
hgdp	rs193922728
ensembl	rs193922728
geneview	rs193922728
scholar	rs193922728
google	rs193922728
pharmgkb	rs193922728
gwascentral	rs193922728
openSNP	rs193922728
23andMe	rs193922728
SNPshot	rs193922728
SNPdbe	rs193922728
MSV3d	rs193922728
GWAS Ctlg	rs193922728

Max Magnitude

0

ClinVar
Risk	rs193922728(A;A)
Alt	rs193922728(A;A)
Reference	Rs193922728(G;G)
Significance	Probable-Pathogenic
Disease	Cardiac arrhythmia not specified
Variation	info
Gene	SCN1B
CLNDBN	Cardiac arrhythmia not specified
Reversed	0
HGVS	NC_000019.9:g.35524946G>A
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030436.1, RCV000454426.1,