rs786204421

Orientation

plus

Stabilized

plus

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

Make rs786204421(-;-)

Make rs786204421(-;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

107663410

Gene	SLC26A4, SLC26A4-AS1

is a	snp
is	mentioned by
dbSNP	rs786204421
dbSNP (classic)	rs786204421
ClinGen	rs786204421
ebi	rs786204421
HLI	rs786204421
Exac	rs786204421
Gnomad	rs786204421
Varsome	rs786204421
LitVar	rs786204421
Map	rs786204421
PheGenI	rs786204421
Biobank	rs786204421
1000 genomes	rs786204421
hgdp	rs786204421
ensembl	rs786204421
geneview	rs786204421
scholar	rs786204421
google	rs786204421
pharmgkb	rs786204421
gwascentral	rs786204421
openSNP	rs786204421
23andMe	rs786204421
SNPshot	rs786204421
SNPdbe	rs786204421
MSV3d	rs786204421
GWAS Ctlg	rs786204421

Max Magnitude

0

ClinVar
Risk	rs786204421(-;-)
Alt	rs786204421(-;-)
Reference	Rs786204421(T;T)
Significance	Probable-Pathogenic
Disease	Pendred's syndrome
Variation	info
Gene	SLC26A4-AS1 SLC26A4
CLNDBN	Pendred's syndrome
Reversed	0
HGVS	NC_000007.13:g.107303855delT
CLNSRC
CLNACC	RCV000169009.1,