rs527236156

Orientation

plus

Stabilized

plus

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

Make rs527236156(C;T)

Make rs527236156(T;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

21703981

Gene

KCNJ18

is a	snp
is	mentioned by
dbSNP	rs527236156
dbSNP (classic)	rs527236156
ClinGen	rs527236156
ebi	rs527236156
HLI	rs527236156
Exac	rs527236156
Gnomad	rs527236156
Varsome	rs527236156
LitVar	rs527236156
Map	rs527236156
PheGenI	rs527236156
Biobank	rs527236156
1000 genomes	rs527236156
hgdp	rs527236156
ensembl	rs527236156
geneview	rs527236156
scholar	rs527236156
google	rs527236156
pharmgkb	rs527236156
gwascentral	rs527236156
openSNP	rs527236156
23andMe	rs527236156
SNPshot	rs527236156
SNPdbe	rs527236156
MSV3d	rs527236156
GWAS Ctlg	rs527236156

Max Magnitude

0

ClinVar
Risk	rs527236156(T;T)
Alt	rs527236156(T;T)
Reference	Rs527236156(C;C)
Significance	Pathogenic
Disease	Thyrotoxic periodic paralysis
Variation	info
Gene	KCNJ18
CLNDBN	Thyrotoxic periodic paralysis
Reversed	0
HGVS	NC_000017.11:g.21703981C>T
CLNSRC	ClinVar
CLNACC	RCV000132743.2,