rs786204742

Merged into

rs752807925

Orientation

plus

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

Make rs786204742(C;T)

Make rs786204742(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

107704382

Gene

SLC26A4

is a	snp
is	mentioned by
dbSNP	rs786204742
dbSNP (classic)	rs786204742
ClinGen	rs786204742
ebi	rs786204742
HLI	rs786204742
Exac	rs786204742
Gnomad	rs786204742
Varsome	rs786204742
LitVar	rs786204742
Map	rs786204742
PheGenI	rs786204742
Biobank	rs786204742
1000 genomes	rs786204742
hgdp	rs786204742
ensembl	rs786204742
geneview	rs786204742
scholar	rs786204742
google	rs786204742
pharmgkb	rs786204742
gwascentral	rs786204742
openSNP	rs786204742
23andMe	rs786204742
SNPshot	rs786204742
SNPdbe	rs786204742
MSV3d	rs786204742
GWAS Ctlg	rs786204742

Status

Merged into rs752807925

Max Magnitude

0

ClinVar
Risk	rs786204742(T;T)
Alt	rs786204742(T;T)
Reference	Rs786204742(C;C)
Significance	Probable-Pathogenic
Disease	Pendred's syndrome
Variation	info
Gene	SLC26A4
CLNDBN	Pendred's syndrome
Reversed	0
HGVS	NC_000007.14:g.107704382C>T
CLNSRC
CLNACC	RCV000169591.1,