rs267607029

Orientation

plus

Stabilized

plus

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

Make rs267607029(A;A)

Make rs267607029(A;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

35033828

Gene

SCN1B

is a	snp
is	mentioned by
dbSNP	rs267607029
dbSNP (classic)	rs267607029
ClinGen	rs267607029
ebi	rs267607029
HLI	rs267607029
Exac	rs267607029
Gnomad	rs267607029
Varsome	rs267607029
LitVar	rs267607029
Map	rs267607029
PheGenI	rs267607029
Biobank	rs267607029
1000 genomes	rs267607029
hgdp	rs267607029
ensembl	rs267607029
geneview	rs267607029
scholar	rs267607029
google	rs267607029
pharmgkb	rs267607029
gwascentral	rs267607029
openSNP	rs267607029
23andMe	rs267607029
SNPshot	rs267607029
SNPdbe	rs267607029
MSV3d	rs267607029
GWAS Ctlg	rs267607029

Max Magnitude

0

ClinVar
Risk	rs267607029(A;A)
Alt	rs267607029(A;A)
Reference	Rs267607029(G;G)
Significance	Pathogenic
Disease	Cardiac conduction defect
Variation	info
Gene	SCN1B
CLNDBN	Cardiac conduction defect, nonspecific
Reversed	0
HGVS	NC_000019.9:g.35524732G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009838.2,