rs201889708

Orientation

plus

Stabilized

plus

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

Make rs201889708(A;A)

Make rs201889708(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

81143400

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs201889708
dbSNP (classic)	rs201889708
ClinGen	rs201889708
ebi	rs201889708
HLI	rs201889708
Exac	rs201889708
Gnomad	rs201889708
Varsome	rs201889708
LitVar	rs201889708
Map	rs201889708
PheGenI	rs201889708
Biobank	rs201889708
1000 genomes	rs201889708
hgdp	rs201889708
ensembl	rs201889708
geneview	rs201889708
scholar	rs201889708
google	rs201889708
pharmgkb	rs201889708
gwascentral	rs201889708
openSNP	rs201889708
23andMe	rs201889708
SNPshot	rs201889708
SNPdbe	rs201889708
MSV3d	rs201889708
GWAS Ctlg	rs201889708

Max Magnitude

0

ClinVar
Risk	rs201889708(A;A)
Alt	rs201889708(A;A)
Reference	Rs201889708(G;G)
Significance	Probable-Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	LOC101928431 TSHR
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000014.8:g.81609744G>A
CLNSRC
CLNACC	RCV000190814.1,