rs1057516636

Orientation

plus

Stabilized

plus

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

Make rs1057516636(-;-)

Make rs1057516636(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

107701989

Gene

SLC26A4

is a	snp
is	mentioned by
dbSNP	rs1057516636
dbSNP (classic)	rs1057516636
ClinGen	rs1057516636
ebi	rs1057516636
HLI	rs1057516636
Exac	rs1057516636
Gnomad	rs1057516636
Varsome	rs1057516636
LitVar	rs1057516636
Map	rs1057516636
PheGenI	rs1057516636
Biobank	rs1057516636
1000 genomes	rs1057516636
hgdp	rs1057516636
ensembl	rs1057516636
geneview	rs1057516636
scholar	rs1057516636
google	rs1057516636
pharmgkb	rs1057516636
gwascentral	rs1057516636
openSNP	rs1057516636
23andMe	rs1057516636
SNPshot	rs1057516636
SNPdbe	rs1057516636
MSV3d	rs1057516636
GWAS Ctlg	rs1057516636

Max Magnitude

0

ClinVar
Risk	rs1057516636(-;-)
Alt	rs1057516636(-;-)
Reference	Rs1057516636(C;C)
Significance	Probable-Pathogenic
Disease	Pendred's syndrome
Variation	info
Gene	SLC26A4
CLNDBN	Pendred's syndrome
Reversed	0
HGVS	NC_000007.13:g.107342434delC
CLNSRC
CLNACC	RCV000412428.1,