rs140348243

Orientation

plus

Stabilized

plus

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

Make rs140348243(A;A)

Make rs140348243(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

118137097

Gene

SCN4B

is a	snp
is	mentioned by
dbSNP	rs140348243
dbSNP (classic)	rs140348243
ClinGen	rs140348243
ebi	rs140348243
HLI	rs140348243
Exac	rs140348243
Gnomad	rs140348243
Varsome	rs140348243
LitVar	rs140348243
Map	rs140348243
PheGenI	rs140348243
Biobank	rs140348243
1000 genomes	rs140348243
hgdp	rs140348243
ensembl	rs140348243
geneview	rs140348243
scholar	rs140348243
google	rs140348243
pharmgkb	rs140348243
gwascentral	rs140348243
openSNP	rs140348243
23andMe	rs140348243
SNPshot	rs140348243
SNPdbe	rs140348243
MSV3d	rs140348243
GWAS Ctlg	rs140348243

Max Magnitude

0

ClinVar
Risk	rs140348243(A;A)
Alt	rs140348243(A;A)
Reference	Rs140348243(G;G)
Significance	Probable-Pathogenic
Disease	SUDDEN INFANT DEATH SYNDROME Long QT syndrome 10 not provided
Variation	info
Gene	SCN4B
CLNDBN	SUDDEN INFANT DEATH SYNDROME Long QT syndrome 10 not provided
Reversed	0
HGVS	NC_000011.9:g.118007812G>A
CLNSRC
CLNACC	RCV000171568.1, RCV000234662.1, RCV000490150.1,