rs760874290

Orientation

plus

Stabilized

plus

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

Make rs760874290(C;C)

Make rs760874290(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

14

Position

81091070

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs760874290
dbSNP (classic)	rs760874290
ClinGen	rs760874290
ebi	rs760874290
HLI	rs760874290
Exac	rs760874290
Gnomad	rs760874290
Varsome	rs760874290
LitVar	rs760874290
Map	rs760874290
PheGenI	rs760874290
Biobank	rs760874290
1000 genomes	rs760874290
hgdp	rs760874290
ensembl	rs760874290
geneview	rs760874290
scholar	rs760874290
google	rs760874290
pharmgkb	rs760874290
gwascentral	rs760874290
openSNP	rs760874290
23andMe	rs760874290
SNPshot	rs760874290
SNPdbe	rs760874290
MSV3d	rs760874290
GWAS Ctlg	rs760874290

Max Magnitude

0

ClinVar
Risk	rs760874290(C;C)
Alt	rs760874290(C;C)
Reference	Rs760874290(G;G)
Significance	Probable-Pathogenic
Disease	Hyperthyroidism Congenital hypothyroidism not provided
Variation	info
Gene	LOC101928462 TSHR
CLNDBN	Hyperthyroidism, nonautoimmune Congenital hypothyroidism not provided
Reversed	0
HGVS	NC_000014.8:g.81557414G>C
CLNSRC
CLNACC	RCV000308671.1, RCV000400375.1, RCV000489665.1,