rs199473656

Orientation

plus

Stabilized

plus

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

Make rs199473656(C;C)

Make rs199473656(C;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70175689

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs199473656
dbSNP (classic)	rs199473656
ClinGen	rs199473656
ebi	rs199473656
HLI	rs199473656
Exac	rs199473656
Gnomad	rs199473656
Varsome	rs199473656
LitVar	rs199473656
Map	rs199473656
PheGenI	rs199473656
Biobank	rs199473656
1000 genomes	rs199473656
hgdp	rs199473656
ensembl	rs199473656
geneview	rs199473656
scholar	rs199473656
google	rs199473656
pharmgkb	rs199473656
gwascentral	rs199473656
openSNP	rs199473656
23andMe	rs199473656
SNPshot	rs199473656
SNPdbe	rs199473656
MSV3d	rs199473656
GWAS Ctlg	rs199473656

Max Magnitude

0

ClinVar
Risk	rs199473656(C;C)
Alt	rs199473656(C;C)
Reference	Rs199473656(T;T)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNJ2
CLNDBN	Congenital long QT syndrome
Reversed	0
HGVS	NC_000017.10:g.68171830T>C
CLNSRC	ClinVar
CLNACC	RCV000058325.3,