rs121908874

Orientation

plus

Stabilized

plus

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

Make rs121908874(C;C)

Make rs121908874(C;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

81143584

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs121908874
dbSNP (classic)	rs121908874
ClinGen	rs121908874
ebi	rs121908874
HLI	rs121908874
Exac	rs121908874
Gnomad	rs121908874
Varsome	rs121908874
LitVar	rs121908874
Map	rs121908874
PheGenI	rs121908874
Biobank	rs121908874
1000 genomes	rs121908874
hgdp	rs121908874
ensembl	rs121908874
geneview	rs121908874
scholar	rs121908874
google	rs121908874
pharmgkb	rs121908874
gwascentral	rs121908874
openSNP	rs121908874
23andMe	rs121908874
SNPshot	rs121908874
SNPdbe	rs121908874
MSV3d	rs121908874
GWAS Ctlg	rs121908874

Max Magnitude

0

OMIM	603372
Desc
Variant	0019
Related	also

ClinVar
Risk	rs121908874(C;C)
Alt	rs121908874(C;C)
Reference	Rs121908874(T;T)
Significance	Pathogenic
Disease	Hyperthyroidism
Variation	info
Gene	LOC101928431 TSHR
CLNDBN	Hyperthyroidism, nonautoimmune
Reversed	0
HGVS	NC_000014.8:g.81609928T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006818.2,