rs786205806

Orientation

plus

Stabilized

plus

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

Make rs786205806(A;A)

Make rs786205806(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

21

Position

34364156

Gene	KCNE2, LOC105372791

is a	snp
is	mentioned by
dbSNP	rs786205806
dbSNP (classic)	rs786205806
ClinGen	rs786205806
ebi	rs786205806
HLI	rs786205806
Exac	rs786205806
Gnomad	rs786205806
Varsome	rs786205806
LitVar	rs786205806
Map	rs786205806
PheGenI	rs786205806
Biobank	rs786205806
1000 genomes	rs786205806
hgdp	rs786205806
ensembl	rs786205806
geneview	rs786205806
scholar	rs786205806
google	rs786205806
pharmgkb	rs786205806
gwascentral	rs786205806
openSNP	rs786205806
23andMe	rs786205806
SNPshot	rs786205806
SNPdbe	rs786205806
MSV3d	rs786205806
GWAS Ctlg	rs786205806

Max Magnitude

0

ClinVar
Risk	rs786205806(A;A)
Alt	rs786205806(A;A)
Reference	Rs786205806(G;G)
Significance	Probable-Pathogenic
Disease	Familial atrial fibrillation Romano-Ward syndrome Long QT syndrome
Variation	info
Gene	KCNE2
CLNDBN	Familial atrial fibrillation Romano-Ward syndrome Long QT syndrome
Reversed	0
HGVS	NC_000021.8:g.35736455G>A
CLNSRC
CLNACC	RCV000288510.1, RCV000331921.1, RCV000381892.1,