rs17215437

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0
(G;G)	0	common in complete genomics

Make rs17215437(A;A)

Make rs17215437(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

74457316

Gene

KCNE3

is a	snp
is	mentioned by
dbSNP	rs17215437
dbSNP (classic)	rs17215437
ClinGen	rs17215437
ebi	rs17215437
HLI	rs17215437
Exac	rs17215437
Gnomad	rs17215437
Varsome	rs17215437
LitVar	rs17215437
Map	rs17215437
PheGenI	rs17215437
Biobank	rs17215437
1000 genomes	rs17215437
hgdp	rs17215437
ensembl	rs17215437
geneview	rs17215437
scholar	rs17215437
google	rs17215437
pharmgkb	rs17215437
gwascentral	rs17215437
openSNP	rs17215437
23andMe	rs17215437
SNPshot	rs17215437
SNPdbe	rs17215437
MSV3d	rs17215437
GWAS Ctlg	rs17215437

GMAF

0.001837

Max Magnitude

0

OMIM	604433
Desc	HYPOKALEMIC PERIODIC PARALYSIS
Variant	0001
Related	also

ClinVar
Risk	rs17215437(A;A)
Alt	rs17215437(A;A)
Reference	Rs17215437(G;G)
Significance	Other
Disease	not provided Periodic paralysis not specified Cardiovascular phenotype Syncope Ventricular fibrillation
Variation	info
Gene	KCNE3
CLNDBN	not provided Periodic paralysis not specified Cardiovascular phenotype Syncope Ventricular fibrillation
Reversed	1
HGVS	NC_000011.9:g.74168361C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005879.5, RCV000171813.1, RCV000223897.3, RCV000253742.1, RCV000415218.1,