rs137853071

Orientation

minus

Stabilized

minus

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

Make rs137853071(C;T)

Make rs137853071(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

160041644

Gene

KCNJ10

is a	snp
is	mentioned by
dbSNP	rs137853071
dbSNP (classic)	rs137853071
ClinGen	rs137853071
ebi	rs137853071
HLI	rs137853071
Exac	rs137853071
Gnomad	rs137853071
Varsome	rs137853071
LitVar	rs137853071
Map	rs137853071
PheGenI	rs137853071
Biobank	rs137853071
1000 genomes	rs137853071
hgdp	rs137853071
ensembl	rs137853071
geneview	rs137853071
scholar	rs137853071
google	rs137853071
pharmgkb	rs137853071
gwascentral	rs137853071
openSNP	rs137853071
23andMe	rs137853071
SNPshot	rs137853071
SNPdbe	rs137853071
MSV3d	rs137853071
GWAS Ctlg	rs137853071

Max Magnitude

0

OMIM	602208
Desc
Variant	0006
Related	also

ClinVar
Risk	rs137853071(T;T)
Alt	rs137853071(T;T)
Reference	Rs137853071(C;C)
Significance	Pathogenic
Disease	SeSAME syndrome not provided
Variation	info
Gene	KCNJ10
CLNDBN	SeSAME syndrome not provided
Reversed	1
HGVS	NC_000001.10:g.160011434G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007893.4, RCV000413534.1,