rs1060499808

Orientation

plus

Stabilized

plus

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

Make rs1060499808(C;C)

Make rs1060499808(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

107704344

Gene

SLC26A4

is a	snp
is	mentioned by
dbSNP	rs1060499808
dbSNP (classic)	rs1060499808
ClinGen	rs1060499808
ebi	rs1060499808
HLI	rs1060499808
Exac	rs1060499808
Gnomad	rs1060499808
Varsome	rs1060499808
LitVar	rs1060499808
Map	rs1060499808
PheGenI	rs1060499808
Biobank	rs1060499808
1000 genomes	rs1060499808
hgdp	rs1060499808
ensembl	rs1060499808
geneview	rs1060499808
scholar	rs1060499808
google	rs1060499808
pharmgkb	rs1060499808
gwascentral	rs1060499808
openSNP	rs1060499808
23andMe	rs1060499808
SNPshot	rs1060499808
SNPdbe	rs1060499808
MSV3d	rs1060499808
GWAS Ctlg	rs1060499808

Max Magnitude

0

ClinVar
Risk	rs1060499808(C;C)
Alt	rs1060499808(C;C)
Reference	Rs1060499808(T;T)
Significance	Pathogenic
Disease	Pendred's syndrome
Variation	info
Gene	SLC26A4
CLNDBN	Pendred's syndrome
Reversed	0
HGVS	NC_000007.13:g.107344789T>C
CLNSRC
CLNACC	RCV000454307.1,