rs137853067

Orientation

minus

Stabilized

minus

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

Make rs137853067(C;T)

Make rs137853067(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

160041938

Gene

KCNJ10

is a	snp
is	mentioned by
dbSNP	rs137853067
dbSNP (classic)	rs137853067
ClinGen	rs137853067
ebi	rs137853067
HLI	rs137853067
Exac	rs137853067
Gnomad	rs137853067
Varsome	rs137853067
LitVar	rs137853067
Map	rs137853067
PheGenI	rs137853067
Biobank	rs137853067
1000 genomes	rs137853067
hgdp	rs137853067
ensembl	rs137853067
geneview	rs137853067
scholar	rs137853067
google	rs137853067
pharmgkb	rs137853067
gwascentral	rs137853067
openSNP	rs137853067
23andMe	rs137853067
SNPshot	rs137853067
SNPdbe	rs137853067
MSV3d	rs137853067
GWAS Ctlg	rs137853067

Max Magnitude

0

OMIM	602208
Desc
Variant	0002
Related	also

ClinVar
Risk	rs137853067(T;T)
Alt	rs137853067(T;T)
Reference	Rs137853067(C;C)
Significance	Pathogenic
Disease	SeSAME syndrome
Variation	info
Gene	KCNJ10
CLNDBN	SeSAME syndrome
Reversed	1
HGVS	NC_000001.10:g.160011728G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007889.4,