rs199473377

Orientation

plus

Stabilized

plus

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

Make rs199473377(C;C)

Make rs199473377(C;G)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70175470

Gene

KCNJ2

is a	snp
is	mentioned by
dbSNP	rs199473377
dbSNP (classic)	rs199473377
ClinGen	rs199473377
ebi	rs199473377
HLI	rs199473377
Exac	rs199473377
Gnomad	rs199473377
Varsome	rs199473377
LitVar	rs199473377
Map	rs199473377
PheGenI	rs199473377
Biobank	rs199473377
1000 genomes	rs199473377
hgdp	rs199473377
ensembl	rs199473377
geneview	rs199473377
scholar	rs199473377
google	rs199473377
pharmgkb	rs199473377
gwascentral	rs199473377
openSNP	rs199473377
23andMe	rs199473377
SNPshot	rs199473377
SNPdbe	rs199473377
MSV3d	rs199473377
GWAS Ctlg	rs199473377

Max Magnitude

0

ClinVar
Risk	rs199473377(A;A) rs199473377(C;C)
Alt	rs199473377(A;A) rs199473377(C;C)
Reference	Rs199473377(G;G)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNJ2
CLNDBN	Congenital long QT syndrome
Reversed	0
HGVS	NC_000017.10:g.68171611G>A; NC_000017.10:g.68171611G>C
CLNSRC	ClinVar
CLNACC	RCV000058312.3, RCV000058313.3,