rs1057517298

Orientation

plus

Stabilized

plus

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

Make rs1057517298(G;T)

Make rs1057517298(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

107694620

Gene

SLC26A4

is a	snp
is	mentioned by
dbSNP	rs1057517298
dbSNP (classic)	rs1057517298
ClinGen	rs1057517298
ebi	rs1057517298
HLI	rs1057517298
Exac	rs1057517298
Gnomad	rs1057517298
Varsome	rs1057517298
LitVar	rs1057517298
Map	rs1057517298
PheGenI	rs1057517298
Biobank	rs1057517298
1000 genomes	rs1057517298
hgdp	rs1057517298
ensembl	rs1057517298
geneview	rs1057517298
scholar	rs1057517298
google	rs1057517298
pharmgkb	rs1057517298
gwascentral	rs1057517298
openSNP	rs1057517298
23andMe	rs1057517298
SNPshot	rs1057517298
SNPdbe	rs1057517298
MSV3d	rs1057517298
GWAS Ctlg	rs1057517298

Max Magnitude

0

ClinVar
Risk	rs1057517298(T;T)
Alt	rs1057517298(T;T)
Reference	Rs1057517298(G;G)
Significance	Probable-Pathogenic
Disease	Pendred's syndrome
Variation	info
Gene	SLC26A4
CLNDBN	Pendred's syndrome
Reversed	0
HGVS	NC_000007.13:g.107335065G>T
CLNSRC
CLNACC	RCV000410038.1,