rs752807925

Orientation

plus

Stabilized

plus

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

Make rs752807925(C;T)

Make rs752807925(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

107704382

Gene

SLC26A4

is a	snp
is	mentioned by
dbSNP	rs752807925
dbSNP (classic)	rs752807925
ClinGen	rs752807925
ebi	rs752807925
HLI	rs752807925
Exac	rs752807925
Gnomad	rs752807925
Varsome	rs752807925
LitVar	rs752807925
Map	rs752807925
PheGenI	rs752807925
Biobank	rs752807925
1000 genomes	rs752807925
hgdp	rs752807925
ensembl	rs752807925
geneview	rs752807925
scholar	rs752807925
google	rs752807925
pharmgkb	rs752807925
gwascentral	rs752807925
openSNP	rs752807925
23andMe	rs752807925
SNPshot	rs752807925
SNPdbe	rs752807925
MSV3d	rs752807925
GWAS Ctlg	rs752807925

Merged from

Rs786204742

Max Magnitude

0

ClinVar
Risk	rs752807925(T;T)
Alt	rs752807925(T;T)
Reference	Rs752807925(C;C)
Significance	Probable-Pathogenic
Disease	Pendred's syndrome
Variation	info
Gene	SLC26A4
CLNDBN	Pendred's syndrome
Reversed	0
HGVS	NC_000007.13:g.107344827C>T
CLNSRC
CLNACC	RCV000169591.1,