rs121908864

Orientation

plus

Stabilized

plus

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

Make rs121908864(C;C)

Make rs121908864(C;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

81143416

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs121908864
dbSNP (classic)	rs121908864
ClinGen	rs121908864
ebi	rs121908864
HLI	rs121908864
Exac	rs121908864
Gnomad	rs121908864
Varsome	rs121908864
LitVar	rs121908864
Map	rs121908864
PheGenI	rs121908864
Biobank	rs121908864
1000 genomes	rs121908864
hgdp	rs121908864
ensembl	rs121908864
geneview	rs121908864
scholar	rs121908864
google	rs121908864
pharmgkb	rs121908864
gwascentral	rs121908864
openSNP	rs121908864
23andMe	rs121908864
SNPshot	rs121908864
SNPdbe	rs121908864
MSV3d	rs121908864
GWAS Ctlg	rs121908864

Max Magnitude

0

OMIM	603372
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121908864(C;C)
Alt	rs121908864(C;C)
Reference	Rs121908864(T;T)
Significance	Pathogenic
Disease	Hyperthyroidism
Variation	info
Gene	LOC101928431 TSHR
CLNDBN	Hyperthyroidism, nonautoimmune
Reversed	0
HGVS	NC_000014.8:g.81609760T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006806.2,