rs786205822

Orientation

plus

Stabilized

plus

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

Make rs786205822(-;-)

Make rs786205822(-;GCC)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

70175955

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs786205822
dbSNP (classic)	rs786205822
ClinGen	rs786205822
ebi	rs786205822
HLI	rs786205822
Exac	rs786205822
Gnomad	rs786205822
Varsome	rs786205822
LitVar	rs786205822
Map	rs786205822
PheGenI	rs786205822
Biobank	rs786205822
1000 genomes	rs786205822
hgdp	rs786205822
ensembl	rs786205822
geneview	rs786205822
scholar	rs786205822
google	rs786205822
pharmgkb	rs786205822
gwascentral	rs786205822
openSNP	rs786205822
23andMe	rs786205822
SNPshot	rs786205822
SNPdbe	rs786205822
MSV3d	rs786205822
GWAS Ctlg	rs786205822

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs786205822(GCC;GCC)
Significance	Probable-Pathogenic
Disease	Cardiac arrhythmia
Variation	info
Gene	KCNJ2
CLNDBN	Cardiac arrhythmia
Reversed	0
HGVS	NC_000017.10:g.68172096_68172098delGCC
CLNSRC
CLNACC	RCV000170997.2,