rs1057519457

Orientation

plus

Stabilized

plus

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

Make rs1057519457(A;T)

Make rs1057519457(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

19

Position

35033599

Gene

SCN1B

is a	snp
is	mentioned by
dbSNP	rs1057519457
dbSNP (classic)	rs1057519457
ClinGen	rs1057519457
ebi	rs1057519457
HLI	rs1057519457
Exac	rs1057519457
Gnomad	rs1057519457
Varsome	rs1057519457
LitVar	rs1057519457
Map	rs1057519457
PheGenI	rs1057519457
Biobank	rs1057519457
1000 genomes	rs1057519457
hgdp	rs1057519457
ensembl	rs1057519457
geneview	rs1057519457
scholar	rs1057519457
google	rs1057519457
pharmgkb	rs1057519457
gwascentral	rs1057519457
openSNP	rs1057519457
23andMe	rs1057519457
SNPshot	rs1057519457
SNPdbe	rs1057519457
MSV3d	rs1057519457
GWAS Ctlg	rs1057519457

Max Magnitude

0

ClinVar
Risk	rs1057519457(T;T)
Alt	rs1057519457(T;T)
Reference	Rs1057519457(A;A)
Significance	Pathogenic
Disease	Cardiomyopathy
Variation	info
Gene	SCN1B
CLNDBN	Cardiomyopathy
Reversed	0
HGVS	NC_000019.9:g.35524503A>T
CLNSRC
CLNACC	RCV000416448.1,