rs150401343

Orientation

plus

Stabilized

plus

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

Make rs150401343(A;A)

Make rs150401343(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

111780713

Gene

KCND3

is a	snp
is	mentioned by
dbSNP	rs150401343
dbSNP (classic)	rs150401343
ClinGen	rs150401343
ebi	rs150401343
HLI	rs150401343
Exac	rs150401343
Gnomad	rs150401343
Varsome	rs150401343
LitVar	rs150401343
Map	rs150401343
PheGenI	rs150401343
Biobank	rs150401343
1000 genomes	rs150401343
hgdp	rs150401343
ensembl	rs150401343
geneview	rs150401343
scholar	rs150401343
google	rs150401343
pharmgkb	rs150401343
gwascentral	rs150401343
openSNP	rs150401343
23andMe	rs150401343
SNPshot	rs150401343
SNPdbe	rs150401343
MSV3d	rs150401343
GWAS Ctlg	rs150401343

Max Magnitude

0

ClinVar
Risk	rs150401343(A;A)
Alt	rs150401343(A;A)
Reference	Rs150401343(G;G)
Significance	Pathogenic
Disease	Brugada syndrome 9 not provided
Variation	info
Gene	KCND3
CLNDBN	Brugada syndrome 9 not provided
Reversed	0
HGVS	NC_000001.10:g.112323335G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000172842.3, RCV000415916.1,