rs146281367

Orientation

plus

Stabilized

plus

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

Make rs146281367(A;A)

Make rs146281367(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

107683537

Gene

SLC26A4

is a	snp
is	mentioned by
dbSNP	rs146281367
dbSNP (classic)	rs146281367
ClinGen	rs146281367
ebi	rs146281367
HLI	rs146281367
Exac	rs146281367
Gnomad	rs146281367
Varsome	rs146281367
LitVar	rs146281367
Map	rs146281367
PheGenI	rs146281367
Biobank	rs146281367
1000 genomes	rs146281367
hgdp	rs146281367
ensembl	rs146281367
geneview	rs146281367
scholar	rs146281367
google	rs146281367
pharmgkb	rs146281367
gwascentral	rs146281367
openSNP	rs146281367
23andMe	rs146281367
SNPshot	rs146281367
SNPdbe	rs146281367
MSV3d	rs146281367
GWAS Ctlg	rs146281367

Max Magnitude

0

ClinVar
Risk	rs146281367(A;A) rs146281367(C;C) rs146281367(T;T)
Alt	rs146281367(A;A) rs146281367(C;C) rs146281367(T;T)
Reference	Rs146281367(G;G)
Significance	Other
Disease	Pendred's syndrome
Variation	info
Gene	SLC26A4
CLNDBN	Pendred's syndrome
Reversed	0
HGVS	NC_000007.13:g.107323982G>T
CLNSRC
CLNACC	RCV000169430.2,