rs189261858

Orientation

plus

Stabilized

plus

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

Make rs189261858(A;A)

Make rs189261858(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

14

Position

81143407

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs189261858
dbSNP (classic)	rs189261858
ClinGen	rs189261858
ebi	rs189261858
HLI	rs189261858
Exac	rs189261858
Gnomad	rs189261858
Varsome	rs189261858
LitVar	rs189261858
Map	rs189261858
PheGenI	rs189261858
Biobank	rs189261858
1000 genomes	rs189261858
hgdp	rs189261858
ensembl	rs189261858
geneview	rs189261858
scholar	rs189261858
google	rs189261858
pharmgkb	rs189261858
gwascentral	rs189261858
openSNP	rs189261858
23andMe	rs189261858
SNPshot	rs189261858
SNPdbe	rs189261858
MSV3d	rs189261858
GWAS Ctlg	rs189261858

Max Magnitude

0

ClinVar
Risk	rs189261858(A;A)
Alt	rs189261858(A;A)
Reference	Rs189261858(G;G)
Significance	Pathogenic
Disease	not provided Hypothyroidism
Variation	info
Gene	LOC101928431 TSHR
CLNDBN	not provided Hypothyroidism, congenital, nongoitrous, 1
Reversed	0
HGVS	NC_000014.8:g.81609751G>A
CLNSRC
CLNACC	RCV000273881.1, RCV000490528.1,