rs121908873

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs121908873(G;T)

Make rs121908873(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

81139828

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs121908873
dbSNP (classic)	rs121908873
ClinGen	rs121908873
ebi	rs121908873
HLI	rs121908873
Exac	rs121908873
Gnomad	rs121908873
Varsome	rs121908873
LitVar	rs121908873
Map	rs121908873
PheGenI	rs121908873
Biobank	rs121908873
1000 genomes	rs121908873
hgdp	rs121908873
ensembl	rs121908873
geneview	rs121908873
scholar	rs121908873
google	rs121908873
pharmgkb	rs121908873
gwascentral	rs121908873
openSNP	rs121908873
23andMe	rs121908873
SNPshot	rs121908873
SNPdbe	rs121908873
MSV3d	rs121908873
GWAS Ctlg	rs121908873

Merged from

Rs121908878

Max Magnitude

0

OMIM	603372
Desc
Variant	0017
Related	also

ClinVar
Risk	rs121908873(A;A) rs121908873(T;T)
Alt	rs121908873(A;A) rs121908873(T;T)
Reference	Rs121908873(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.81606172G>A; NC_000014.8:g.81606172G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006823.2, RCV000006816.4,