rs1057516678

Orientation

plus

Stabilized

plus

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

Make rs1057516678(C;T)

Make rs1057516678(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

107674963

Gene

SLC26A4

is a	snp
is	mentioned by
dbSNP	rs1057516678
dbSNP (classic)	rs1057516678
ClinGen	rs1057516678
ebi	rs1057516678
HLI	rs1057516678
Exac	rs1057516678
Gnomad	rs1057516678
Varsome	rs1057516678
LitVar	rs1057516678
Map	rs1057516678
PheGenI	rs1057516678
Biobank	rs1057516678
1000 genomes	rs1057516678
hgdp	rs1057516678
ensembl	rs1057516678
geneview	rs1057516678
scholar	rs1057516678
google	rs1057516678
pharmgkb	rs1057516678
gwascentral	rs1057516678
openSNP	rs1057516678
23andMe	rs1057516678
SNPshot	rs1057516678
SNPdbe	rs1057516678
MSV3d	rs1057516678
GWAS Ctlg	rs1057516678

Max Magnitude

0

ClinVar
Risk	rs1057516678(T;T)
Alt	rs1057516678(T;T)
Reference	Rs1057516678(C;C)
Significance	Probable-Pathogenic
Disease	Pendred's syndrome
Variation	info
Gene	SLC26A4
CLNDBN	Pendred's syndrome
Reversed	0
HGVS	NC_000007.13:g.107315408C>T
CLNSRC
CLNACC	RCV000411641.1,