rs786204502

Orientation

plus

Stabilized

plus

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

Make rs786204502(A;A)

Make rs786204502(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

107701942

Gene

SLC26A4

is a	snp
is	mentioned by
dbSNP	rs786204502
dbSNP (classic)	rs786204502
ClinGen	rs786204502
ebi	rs786204502
HLI	rs786204502
Exac	rs786204502
Gnomad	rs786204502
Varsome	rs786204502
LitVar	rs786204502
Map	rs786204502
PheGenI	rs786204502
Biobank	rs786204502
1000 genomes	rs786204502
hgdp	rs786204502
ensembl	rs786204502
geneview	rs786204502
scholar	rs786204502
google	rs786204502
pharmgkb	rs786204502
gwascentral	rs786204502
openSNP	rs786204502
23andMe	rs786204502
SNPshot	rs786204502
SNPdbe	rs786204502
MSV3d	rs786204502
GWAS Ctlg	rs786204502

Max Magnitude

0

ClinVar
Risk	rs786204502(A;A)
Alt	rs786204502(A;A)
Reference	Rs786204502(G;G)
Significance	Probable-Pathogenic
Disease	Pendred's syndrome
Variation	info
Gene	SLC26A4
CLNDBN	Pendred's syndrome
Reversed	0
HGVS	NC_000007.13:g.107342387G>A
CLNSRC
CLNACC	RCV000169184.1,