rs786205867

Orientation

minus

Stabilized

minus

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

Make rs786205867(A;A)

Make rs786205867(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

111787039

Gene

KCND3

is a	snp
is	mentioned by
dbSNP	rs786205867
dbSNP (classic)	rs786205867
ClinGen	rs786205867
ebi	rs786205867
HLI	rs786205867
Exac	rs786205867
Gnomad	rs786205867
Varsome	rs786205867
LitVar	rs786205867
Map	rs786205867
PheGenI	rs786205867
Biobank	rs786205867
1000 genomes	rs786205867
hgdp	rs786205867
ensembl	rs786205867
geneview	rs786205867
scholar	rs786205867
google	rs786205867
pharmgkb	rs786205867
gwascentral	rs786205867
openSNP	rs786205867
23andMe	rs786205867
SNPshot	rs786205867
SNPdbe	rs786205867
MSV3d	rs786205867
GWAS Ctlg	rs786205867

Max Magnitude

0

ClinVar
Risk	rs786205867(A;A)
Alt	rs786205867(A;A)
Reference	Rs786205867(G;G)
Significance	Pathogenic
Disease	Brugada syndrome 9 not provided Spinocerebellar ataxia 19
Variation	info
Gene	KCND3
CLNDBN	Brugada syndrome 9 not provided Spinocerebellar ataxia 19
Reversed	1
HGVS	NC_000001.10:g.112329661C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000172844.3, RCV000444260.1, RCV000460804.1,