rs775803239

Orientation

plus

Stabilized

plus

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

Make rs775803239(A;A)

Make rs775803239(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

15

Position

73323289

Gene

HCN4

is a	snp
is	mentioned by
dbSNP	rs775803239
dbSNP (classic)	rs775803239
ClinGen	rs775803239
ebi	rs775803239
HLI	rs775803239
Exac	rs775803239
Gnomad	rs775803239
Varsome	rs775803239
LitVar	rs775803239
Map	rs775803239
PheGenI	rs775803239
Biobank	rs775803239
1000 genomes	rs775803239
hgdp	rs775803239
ensembl	rs775803239
geneview	rs775803239
scholar	rs775803239
google	rs775803239
pharmgkb	rs775803239
gwascentral	rs775803239
openSNP	rs775803239
23andMe	rs775803239
SNPshot	rs775803239
SNPdbe	rs775803239
MSV3d	rs775803239
GWAS Ctlg	rs775803239

Max Magnitude

0

ClinVar
Risk	rs775803239(A;A) rs775803239(T;T)
Alt	rs775803239(A;A) rs775803239(T;T)
Reference	Rs775803239(G;G)
Significance	Probable-Pathogenic
Disease	not provided not specified Brugada syndrome 8
Variation	info
Gene	HCN4
CLNDBN	not provided not specified Brugada syndrome 8
Reversed	0
HGVS	NC_000015.9:g.73615630G>A
CLNSRC
CLNACC	RCV000170943.2, RCV000223698.2, RCV000473328.1,