rs121908877

Orientation

plus

Stabilized

plus

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

Make rs121908877(G;T)

Make rs121908877(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

81143945

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs121908877
dbSNP (classic)	rs121908877
ClinGen	rs121908877
ebi	rs121908877
HLI	rs121908877
Exac	rs121908877
Gnomad	rs121908877
Varsome	rs121908877
LitVar	rs121908877
Map	rs121908877
PheGenI	rs121908877
Biobank	rs121908877
1000 genomes	rs121908877
hgdp	rs121908877
ensembl	rs121908877
geneview	rs121908877
scholar	rs121908877
google	rs121908877
pharmgkb	rs121908877
gwascentral	rs121908877
openSNP	rs121908877
23andMe	rs121908877
SNPshot	rs121908877
SNPdbe	rs121908877
MSV3d	rs121908877
GWAS Ctlg	rs121908877

Max Magnitude

0

OMIM	603372
Desc
Variant	0022
Related	also

ClinVar
Risk	rs121908877(T;T)
Alt	rs121908877(T;T)
Reference	Rs121908877(G;G)
Significance	Pathogenic
Disease	Hyperthyroidism Thyroid adenoma
Variation	info
Gene	LOC101928431 TSHR
CLNDBN	Hyperthyroidism, nonautoimmune Thyroid adenoma, hyperfunctioning
Reversed	0
HGVS	NC_000014.8:g.81610289G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006821.2, RCV000006822.4,