rs138943405

Orientation

plus

Stabilized

plus

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

Make rs138943405(A;A)

Make rs138943405(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

160042457

Gene

KCNJ10

is a	snp
is	mentioned by
dbSNP	rs138943405
dbSNP (classic)	rs138943405
ClinGen	rs138943405
ebi	rs138943405
HLI	rs138943405
Exac	rs138943405
Gnomad	rs138943405
Varsome	rs138943405
LitVar	rs138943405
Map	rs138943405
PheGenI	rs138943405
Biobank	rs138943405
1000 genomes	rs138943405
hgdp	rs138943405
ensembl	rs138943405
geneview	rs138943405
scholar	rs138943405
google	rs138943405
pharmgkb	rs138943405
gwascentral	rs138943405
openSNP	rs138943405
23andMe	rs138943405
SNPshot	rs138943405
SNPdbe	rs138943405
MSV3d	rs138943405
GWAS Ctlg	rs138943405

Max Magnitude

0

ClinVar
Risk	rs138943405(A;A)
Alt	rs138943405(A;A)
Reference	Rs138943405(G;G)
Significance	Probable-Pathogenic
Disease	SeSAME syndrome KCNJ10-Related Disorders
Variation	info
Gene	KCNJ10
CLNDBN	SeSAME syndrome KCNJ10-Related Disorders
Reversed	0
HGVS	NC_000001.10:g.160012247G>A
CLNSRC
CLNACC	RCV000193637.1, RCV000319701.1,