rs1057516953

Orientation

plus

Stabilized

plus

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

Make rs1057516953(C;T)

Make rs1057516953(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

107663412

Gene	SLC26A4, SLC26A4-AS1

is a	snp
is	mentioned by
dbSNP	rs1057516953
dbSNP (classic)	rs1057516953
ClinGen	rs1057516953
ebi	rs1057516953
HLI	rs1057516953
Exac	rs1057516953
Gnomad	rs1057516953
Varsome	rs1057516953
LitVar	rs1057516953
Map	rs1057516953
PheGenI	rs1057516953
Biobank	rs1057516953
1000 genomes	rs1057516953
hgdp	rs1057516953
ensembl	rs1057516953
geneview	rs1057516953
scholar	rs1057516953
google	rs1057516953
pharmgkb	rs1057516953
gwascentral	rs1057516953
openSNP	rs1057516953
23andMe	rs1057516953
SNPshot	rs1057516953
SNPdbe	rs1057516953
MSV3d	rs1057516953
GWAS Ctlg	rs1057516953

Max Magnitude

0

ClinVar
Risk	rs1057516953(T;T)
Alt	rs1057516953(T;T)
Reference	Rs1057516953(C;C)
Significance	Pathogenic
Disease	Pendred's syndrome
Variation	info
Gene	SLC26A4-AS1 SLC26A4
CLNDBN	Pendred's syndrome
Reversed	0
HGVS	NC_000007.13:g.107303857C>T
CLNSRC
CLNACC	RCV000411778.1,