rs121908880

Orientation

plus

Stabilized

plus

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

Make rs121908880(C;T)

Make rs121908880(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

81143973

Gene	LOC101928462, TSHR

is a	snp
is	mentioned by
dbSNP	rs121908880
dbSNP (classic)	rs121908880
ClinGen	rs121908880
ebi	rs121908880
HLI	rs121908880
Exac	rs121908880
Gnomad	rs121908880
Varsome	rs121908880
LitVar	rs121908880
Map	rs121908880
PheGenI	rs121908880
Biobank	rs121908880
1000 genomes	rs121908880
hgdp	rs121908880
ensembl	rs121908880
geneview	rs121908880
scholar	rs121908880
google	rs121908880
pharmgkb	rs121908880
gwascentral	rs121908880
openSNP	rs121908880
23andMe	rs121908880
SNPshot	rs121908880
SNPdbe	rs121908880
MSV3d	rs121908880
GWAS Ctlg	rs121908880

Max Magnitude

0

OMIM	603372
Desc
Variant	0025
Related	also

ClinVar
Risk	rs121908880(T;T)
Alt	rs121908880(T;T)
Reference	Rs121908880(C;C)
Significance	Pathogenic
Disease	Hyperthyroidism
Variation	info
Gene	LOC101928431 TSHR
CLNDBN	Hyperthyroidism, nonautoimmune
Reversed	0
HGVS	NC_000014.8:g.81610317C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006825.2,