rs121434386

Orientation

minus

Stabilized

minus

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

Make rs121434386(C;T)

Make rs121434386(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

118141265

Gene

SCN4B

is a	snp
is	mentioned by
dbSNP	rs121434386
dbSNP (classic)	rs121434386
ClinGen	rs121434386
ebi	rs121434386
HLI	rs121434386
Exac	rs121434386
Gnomad	rs121434386
Varsome	rs121434386
LitVar	rs121434386
Map	rs121434386
PheGenI	rs121434386
Biobank	rs121434386
1000 genomes	rs121434386
hgdp	rs121434386
ensembl	rs121434386
geneview	rs121434386
scholar	rs121434386
google	rs121434386
pharmgkb	rs121434386
gwascentral	rs121434386
openSNP	rs121434386
23andMe	rs121434386
SNPshot	rs121434386
SNPdbe	rs121434386
MSV3d	rs121434386
GWAS Ctlg	rs121434386

Max Magnitude

0

OMIM	608256
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121434386(T;T)
Alt	rs121434386(T;T)
Reference	Rs121434386(C;C)
Significance	Pathogenic
Disease	Long QT syndrome 10
Variation	info
Gene	SCN4B
CLNDBN	Long QT syndrome 10
Reversed	1
HGVS	NC_000011.9:g.118011980G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000002563.2,