rs1057516634

Orientation

plus

Stabilized

plus

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

Make rs1057516634(-;-)

Make rs1057516634(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

107661696

Gene	SLC26A4, SLC26A4-AS1

is a	snp
is	mentioned by
dbSNP	rs1057516634
dbSNP (classic)	rs1057516634
ClinGen	rs1057516634
ebi	rs1057516634
HLI	rs1057516634
Exac	rs1057516634
Gnomad	rs1057516634
Varsome	rs1057516634
LitVar	rs1057516634
Map	rs1057516634
PheGenI	rs1057516634
Biobank	rs1057516634
1000 genomes	rs1057516634
hgdp	rs1057516634
ensembl	rs1057516634
geneview	rs1057516634
scholar	rs1057516634
google	rs1057516634
pharmgkb	rs1057516634
gwascentral	rs1057516634
openSNP	rs1057516634
23andMe	rs1057516634
SNPshot	rs1057516634
SNPdbe	rs1057516634
MSV3d	rs1057516634
GWAS Ctlg	rs1057516634

Max Magnitude

0

ClinVar
Risk	rs1057516634(-;-)
Alt	rs1057516634(-;-)
Reference	Rs1057516634(A;A)
Significance	Probable-Pathogenic
Disease	Pendred's syndrome
Variation	info
Gene	SLC26A4-AS1 SLC26A4
CLNDBN	Pendred's syndrome
Reversed	0
HGVS	NC_000007.13:g.107302141delA
CLNSRC
CLNACC	RCV000410259.1,