rs786204730

Orientation

plus

Stabilized

plus

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

Make rs786204730(-;T)

Make rs786204730(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

107672198

Gene

SLC26A4

is a	snp
is	mentioned by
dbSNP	rs786204730
dbSNP (classic)	rs786204730
ClinGen	rs786204730
ebi	rs786204730
HLI	rs786204730
Exac	rs786204730
Gnomad	rs786204730
Varsome	rs786204730
LitVar	rs786204730
Map	rs786204730
PheGenI	rs786204730
Biobank	rs786204730
1000 genomes	rs786204730
hgdp	rs786204730
ensembl	rs786204730
geneview	rs786204730
scholar	rs786204730
google	rs786204730
pharmgkb	rs786204730
gwascentral	rs786204730
openSNP	rs786204730
23andMe	rs786204730
SNPshot	rs786204730
SNPdbe	rs786204730
MSV3d	rs786204730
GWAS Ctlg	rs786204730

Max Magnitude

0

ClinVar
Risk	rs786204730(T;T)
Alt	rs786204730(T;T)
Reference	Rs786204730(-;-)
Significance	Probable-Pathogenic
Disease	Pendred's syndrome not provided
Variation	info
Gene	SLC26A4
CLNDBN	Pendred's syndrome not provided
Reversed	0
HGVS	NC_000007.13:g.107312643dupT
CLNSRC
CLNACC	RCV000169571.1, RCV000488403.1,