rs1057516717

Orientation

plus

Stabilized

plus

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

Make rs1057516717(A;G)

Make rs1057516717(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

107695931

Gene

SLC26A4

is a	snp
is	mentioned by
dbSNP	rs1057516717
dbSNP (classic)	rs1057516717
ClinGen	rs1057516717
ebi	rs1057516717
HLI	rs1057516717
Exac	rs1057516717
Gnomad	rs1057516717
Varsome	rs1057516717
LitVar	rs1057516717
Map	rs1057516717
PheGenI	rs1057516717
Biobank	rs1057516717
1000 genomes	rs1057516717
hgdp	rs1057516717
ensembl	rs1057516717
geneview	rs1057516717
scholar	rs1057516717
google	rs1057516717
pharmgkb	rs1057516717
gwascentral	rs1057516717
openSNP	rs1057516717
23andMe	rs1057516717
SNPshot	rs1057516717
SNPdbe	rs1057516717
MSV3d	rs1057516717
GWAS Ctlg	rs1057516717

Max Magnitude

0

ClinVar
Risk	rs1057516717(G;G)
Alt	rs1057516717(G;G)
Reference	Rs1057516717(A;A)
Significance	Probable-Pathogenic
Disease	Pendred's syndrome
Variation	info
Gene	SLC26A4
CLNDBN	Pendred's syndrome
Reversed	0
HGVS	NC_000007.13:g.107336376A>G
CLNSRC
CLNACC	RCV000411152.1,