rs786204739

Orientation

plus

Stabilized

plus

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

Make rs786204739(G;G)

Make rs786204739(G;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

107698083

Gene

SLC26A4

is a	snp
is	mentioned by
dbSNP	rs786204739
dbSNP (classic)	rs786204739
ClinGen	rs786204739
ebi	rs786204739
HLI	rs786204739
Exac	rs786204739
Gnomad	rs786204739
Varsome	rs786204739
LitVar	rs786204739
Map	rs786204739
PheGenI	rs786204739
Biobank	rs786204739
1000 genomes	rs786204739
hgdp	rs786204739
ensembl	rs786204739
geneview	rs786204739
scholar	rs786204739
google	rs786204739
pharmgkb	rs786204739
gwascentral	rs786204739
openSNP	rs786204739
23andMe	rs786204739
SNPshot	rs786204739
SNPdbe	rs786204739
MSV3d	rs786204739
GWAS Ctlg	rs786204739

Max Magnitude

0

ClinVar
Risk	rs786204739(G;G)
Alt	rs786204739(G;G)
Reference	Rs786204739(T;T)
Significance	Probable-Pathogenic
Disease	Pendred's syndrome
Variation	info
Gene	SLC26A4
CLNDBN	Pendred's syndrome
Reversed	0
HGVS	NC_000007.13:g.107338528T>G
CLNSRC
CLNACC	RCV000169586.1,