rs527236154

Orientation

plus

Stabilized

plus

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

Make rs527236154(A;A)

Make rs527236154(A;G)

Reference

GRCh38 38.1/142

Chromosome

17

Position

21703288

Gene

KCNJ18

is a	snp
is	mentioned by
dbSNP	rs527236154
dbSNP (classic)	rs527236154
ClinGen	rs527236154
ebi	rs527236154
HLI	rs527236154
Exac	rs527236154
Gnomad	rs527236154
Varsome	rs527236154
LitVar	rs527236154
Map	rs527236154
PheGenI	rs527236154
Biobank	rs527236154
1000 genomes	rs527236154
hgdp	rs527236154
ensembl	rs527236154
geneview	rs527236154
scholar	rs527236154
google	rs527236154
pharmgkb	rs527236154
gwascentral	rs527236154
openSNP	rs527236154
23andMe	rs527236154
SNPshot	rs527236154
SNPdbe	rs527236154
MSV3d	rs527236154
GWAS Ctlg	rs527236154

Max Magnitude

0

ClinVar
Risk	rs527236154(A;A)
Alt	rs527236154(A;A)
Reference	Rs527236154(G;G)
Significance	Pathogenic
Disease	Thyrotoxic periodic paralysis
Variation	info
Gene	KCNJ18
CLNDBN	Thyrotoxic periodic paralysis
Reversed	0
HGVS	NC_000017.11:g.21703288G>A
CLNSRC	ClinVar
CLNACC	RCV000132741.2,