rs200546024

Orientation

plus

Stabilized

plus

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

Make rs200546024(A;A)

Make rs200546024(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

73323571

Gene

HCN4

is a	snp
is	mentioned by
dbSNP	rs200546024
dbSNP (classic)	rs200546024
ClinGen	rs200546024
ebi	rs200546024
HLI	rs200546024
Exac	rs200546024
Gnomad	rs200546024
Varsome	rs200546024
LitVar	rs200546024
Map	rs200546024
PheGenI	rs200546024
Biobank	rs200546024
1000 genomes	rs200546024
hgdp	rs200546024
ensembl	rs200546024
geneview	rs200546024
scholar	rs200546024
google	rs200546024
pharmgkb	rs200546024
gwascentral	rs200546024
openSNP	rs200546024
23andMe	rs200546024
SNPshot	rs200546024
SNPdbe	rs200546024
MSV3d	rs200546024
GWAS Ctlg	rs200546024

Max Magnitude

0

ClinVar
Risk	rs200546024(A;A)
Alt	rs200546024(A;A)
Reference	Rs200546024(G;G)
Significance	Pathogenic
Disease	not provided Brugada syndrome 8
Variation	info
Gene	HCN4
CLNDBN	not provided Brugada syndrome 8
Reversed	0
HGVS	NC_000015.9:g.73615912G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000170941.5, RCV000223954.1,