rs786204426

Orientation

plus

Stabilized

plus

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

Make rs786204426(C;C)

Make rs786204426(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

107661644

Gene	SLC26A4, SLC26A4-AS1

is a	snp
is	mentioned by
dbSNP	rs786204426
dbSNP (classic)	rs786204426
ClinGen	rs786204426
ebi	rs786204426
HLI	rs786204426
Exac	rs786204426
Gnomad	rs786204426
Varsome	rs786204426
LitVar	rs786204426
Map	rs786204426
PheGenI	rs786204426
Biobank	rs786204426
1000 genomes	rs786204426
hgdp	rs786204426
ensembl	rs786204426
geneview	rs786204426
scholar	rs786204426
google	rs786204426
pharmgkb	rs786204426
gwascentral	rs786204426
openSNP	rs786204426
23andMe	rs786204426
SNPshot	rs786204426
SNPdbe	rs786204426
MSV3d	rs786204426
GWAS Ctlg	rs786204426

Max Magnitude

0

ClinVar
Risk	rs786204426(C;C)
Alt	rs786204426(C;C)
Reference	Rs786204426(G;G)
Significance	Probable-Pathogenic
Disease	Pendred's syndrome
Variation	info
Gene	SLC26A4-AS1 SLC26A4
CLNDBN	Pendred's syndrome
Reversed	0
HGVS	NC_000007.13:g.107302089G>C
CLNSRC
CLNACC	RCV000169018.1,