rs1057516881

Orientation

plus

Stabilized

plus

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

Make rs1057516881(A;A)

Make rs1057516881(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

107674350

Gene

SLC26A4

is a	snp
is	mentioned by
dbSNP	rs1057516881
dbSNP (classic)	rs1057516881
ClinGen	rs1057516881
ebi	rs1057516881
HLI	rs1057516881
Exac	rs1057516881
Gnomad	rs1057516881
Varsome	rs1057516881
LitVar	rs1057516881
Map	rs1057516881
PheGenI	rs1057516881
Biobank	rs1057516881
1000 genomes	rs1057516881
hgdp	rs1057516881
ensembl	rs1057516881
geneview	rs1057516881
scholar	rs1057516881
google	rs1057516881
pharmgkb	rs1057516881
gwascentral	rs1057516881
openSNP	rs1057516881
23andMe	rs1057516881
SNPshot	rs1057516881
SNPdbe	rs1057516881
MSV3d	rs1057516881
GWAS Ctlg	rs1057516881

Max Magnitude

0

ClinVar
Risk	rs1057516881(A;A)
Alt	rs1057516881(A;A)
Reference	Rs1057516881(T;T)
Significance	Pathogenic
Disease	Pendred's syndrome
Variation	info
Gene	SLC26A4
CLNDBN	Pendred's syndrome
Reversed	0
HGVS	NC_000007.13:g.107314795T>A
CLNSRC
CLNACC	RCV000412454.1,